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« Reply #50 on: August 15, 2007, 06:16:16 PM » |
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Gilchrist & Soames Initiates Urgent Worldwide Toothpaste Voluntary RecallContact: Cindy Duran, Borshoff Johnson Matthews (317) 631-6400, ext. 237 FOR IMMEDIATE RELEASE -- Indianapolis, IN -- August 13, 2007 -- Gilchrist & Soames, an Indianapolis-based provider of toiletry products for the hotel industry, has initiated a worldwide voluntary recall of its Gilchrist & Soames 0.65oz/18ml toothpaste manufactured in China for the company by Ming Fai Enterprises International Co., LTD, after independent tests showed some samples of the toothpaste contained diethylene glycol, or DEG. The United States Food and Drug Administration ("FDA") is not aware of any U.S. reports of poisonings from toothpaste containing DEG. However, the agency is concerned about potential risks from chronic exposure to DEG and exposure to DEG in certain populations, such as children and individuals with kidney or liver disease. DEG in toothpaste has a low but meaningful risk of toxicity and injury to these populations. Toothpaste is not intended to be swallowed, but FDA is concerned about unintentional swallowing or ingestion of toothpaste containing DEG. This voluntary recall is being conducted in cooperation with the FDA. The Company also has notified the Department for Business, Enterprise and Regulatory Reform in the UK to enable it to notify the European Commission to launch a RAPEX notification in the European Union. Hotels in the United States, Canada, Mexico, Bermuda, Barbados, Dominican Republic or Turks & Caicos that received the recalled toothpaste from the company’s United States distribution center, and those located in the U.K., Ireland, Spain, Belgium, France, Italy, Germany, Switzerland and the UAE serviced by the company’s U.K. distribution center, are being asked to destroy any remaining inventory. Hotel guests, who may have received the recalled toothpaste from hotels in any of these countries, should safely dispose of it. "After receiving the FDA alert June 1 about tainted toothpaste manufactured in China, we immediately contacted our two Chinese toothpaste suppliers and initiated a series of independent lab tests in both Hong Kong and the United States to determine the possible presence of DEG," said Kathie De Voe, president of Gilchrist & Soames. At the same time, Gilchrist & Soames stopped all outgoing shipments and quarantined all of its "Made in China" toothpaste. The Company also communicated with all of its hotel clients and suggested that they stop offering Chinese-made Gilchrist & Soames toothpaste to their guests until further investigation and independent testing by Gilchrist & Soames and the FDA. The June 1 FDA Consumer Alert was attached. The Company took these steps even though its toothpaste was not among those cited in the FDA warning. De Voe said, "The fifth round of our independent lab tests showed the presence of DEG in some samples at levels exceeding FDA guidelines from one of our China suppliers. We immediately began the process of initiating a voluntary recall of our complimentary-sized (.65oz/18ml) Gilchrist & Soames toothpaste. We want to ensure that any contaminated toothpaste is safely disposed of and/or destroyed." Gilchrist & Soames is notifying its hotel clients in those countries where the toothpaste was distributed to discard their inventories. The Company is working with each hotel on a guest notification program. Materials will inform guests about this voluntary recall, including the FDA Web address for current toothpaste recalls ( http://www.fda.gov/oc/opacom/hottopics/toothpaste.html), as well as a toll-free telephone number at Gilchrist & Soames U.S. headquarters (1-866-587-6542) that hotel guests may call if they desire more information about the recall. The European Union Web address for further information about toothpaste manufactured in China is http://ec.europa.eu/consumers/dyna/rapex/rapex_archives_en.cfm. Local contact numbers in Europe for Gilchrist & Soames are as follows: Germany – 004908000004988, Ireland – 00353 1800932251, France – 0033 0805114958, Spain – 0034800098797, Switzerland - 0041 0800 001285, Hungary – 0036 0680018077, Italy – 0039 800986779, UK – 08003112139, Belgium – 0032 080048630. De Voe said, "We are thankful that the small size of our tubes (.65oz/18ml) may help reduce the risk. However, we strongly encourage consumers to dispose of any of the recalled toothpaste they may still have." Gilchrist & Soames is working with its global supply chain partners to be certain they meet the standards and specifications outlined in its new testing criteria. New testing to confirm the absence of DEG will be part of that process. This recall is being conducted with the knowledge of the FDA, and the European Authorities.
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« Reply #51 on: August 15, 2007, 06:17:16 PM » |
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Krasniy Oktyabr Inc. Recalls Herring of Special Ambassador "7 Uzlov" Due to Possible Health Risk
Contact:
Krasniy Oktyabr Inc.
718-858-6720
FOR IMMEDIATE RELEASE -- Brooklyn, NY -- August 7, 2007 -- Krasniy Oktyabr Inc., located on 60-20th Street, Brooklyn, NY is recalling packages of Herring of the Special Ambassador "7 Uzlov" because the product may be contaminated with Clostridium botulinum, which can cause botulism, a serious and potentially fatal food borne illness.
The sale of this type of fish is prohibited under New York State Agriculture and Markets regulations because Clostridium botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of botulism poisoning. Symptoms of botulism include blurred or double vision, general weakness, and poor reflexes, difficulty swallowing and respiratory paralysis.
The recalled Herring "7 Uzlov" was distributed to retail stores in NYC. The product comes in metal round containers, 1.3 kg, UPC code: 4-60556-000153. It is a product of Russia.
No illnesses have been reported to date in connection with this problem.
Consumers who have Herring of the Special Ambassador "7 Uzlov" are urged to return it to the place of purchase for a full refund. Consumers with questions should contact the company at 1-718-858-6720.
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« Reply #52 on: August 16, 2007, 06:10:19 PM » |
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Ocean King Enterprises Inc. Recalls the Following Ready-To-Eat Seafood Dips Because of Possible Health Risk
Regal King Premium Krab Dip
Regal King Cajun Krab Dip
Regal King Shrimp Dip
Regal King Smoked Salmon Dip
Contact:
Ocean King Enterprises Inc.
(215) 495-0540
FOR IMMEDIATE RELEASE -- Philadelphia, PA -- August 16, 2007 -- Ocean King Enterprises Inc. of Philadelphia, PA is recalling Ready-to-Eat Seafood Dips, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
Products were distributed through the following A&P warehouses: A&P (C&S) Hatfield in Hatfield, MA; A&P (C&S) Baltimore in North East, MD; and A&P (C&S) Woodbridge in Woodbridge, NJ. Products will have reached consumers through retail stores from warehouse distribution.
The products were sold in bulk 5-pound containers to the warehouses. The dips are then sold in the value added and deli sections of the retail stores in clear plastic containers with a Regal King label. All flavors have a red and white repack label. The brand name is Regal King Gourmet Seafood. The flavors are Premium Krab Dip, Cajun Krab Dip, Shrimp Dip, and Smoked Salmon Dip.
No illnesses have been reported to date.
The recall was the result of an independent systemic sampling program conducted by Ocean King Enterprises Inc. which revealed that one finished product contained the bacteria. The company has ceased the production and distribution of the product as FDA and Ocean King Enterprises continue their investigation as to what caused the problem.
Consumers who purchased Regal King Brand ready-to-eat seafood dips should return the product to the store for a full refund. Consumers with questions may contact Ocean King Enterprises Inc. at (215) 495-0540.
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« Reply #53 on: August 19, 2007, 06:53:03 AM » |
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Confidence Inc. Issues a Voluntary Nationwide Recall in the United States and Canada of One Lot of METABOSLIM Apple Cider Vinegar brand dietary supplement found to contain an Undeclared Drug Ingredient Contact: Confidence Inc. 516-767-1870 FOR IMMEDIATE RELEASE --Port Washington, NY -- August 17, 2007 --- Confidence Inc. of Port Washington, NY, is recalling one lot of METABOSLIMTM Apple Cider Vinegar brand dietary supplement, lot number 3001006, EXP. 102009 and UPC CODE: 92483 00102 because it contains the undeclared drug ingredient sibutramine. This lot was primarily sold in Canada. The product is sold in a plastic bottle with white and red labeling and contains 60 gelatin capsules. The Company has been informed by the Food and Drug Administration (FDA) that lab analysis of METABOSLIMTM samples found that the product contains undeclared sibutramine, an FDA approved drug used as an appetite suppressant for weight loss. The FDA has not approved METABOSLIMTM as a drug; therefore the safety and effectiveness of this product is unknown. FDA advises that this poses a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. No illnesses or injuries have been reported to the company to date in connection with this product. Confidence, Inc. has taken this voluntary action because it is committed to providing accurate information about its products and because of the concern for the health and safety of consumers. Confidence Inc. is working with the FDA in the recall process. It sincerely regrets any inconvenience to customers. Consumers should return any unused METABOSLIMTM for a refund of the full purchase price or price for the unused portion, to the Company's address in Port Washington, NY, or contact Jim Chao at 516-767-1870 or email jim@confidenceusa.com to receive further instructions for returning the product or with any questions.
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« Reply #54 on: August 22, 2007, 06:41:07 PM » |
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Acme Smoked Fish Corporation Recalls Smoked Salmon
Contact:
Acme Smoked Fish Corporation
718-383-8585
FOR IMMEDIATE RELEASE -- Brooklyn, NY -- August 14, 2007 -- Acme Smoked Fish Corporation is voluntarily recalling 132 lbs of 4 oz. Smoked Salmon (Acme NY Original) and 114 lbs of 8 oz. Smoked Salmon (Acme NY Original) with a batch code of 9428 and sell-by-date code of 9-26/2007. This product was distributed to retail stores in the South Florida Region.
The potential for contamination was noted after routine testing by the Florida Department of Agriculture and Consumer Services revealed the presence of Listeria monocytogenes in one 4 ounce package of "4 oz. Smoked Salmon (Acme Y Original)" with product code 9428 and sell-by-date code of 9/26/07. This organism can cause serious complications for pregnant women, young children, frail or elderly people, and others with weakened immune systems.
No illnesses have been reported to date in connection with this problem.
Consumers who have purchased 4 oz. Smoked Salmon (Acme NY Original) and/or 8 oz. Smoked Salmon (Acme NY Original) with batch code 9428 and sell-by-date 9/26/07 are urged to contact Acme for further details and refunds. Consumers with questions may contact the Quality Assurance Department at Acme Smoked Fish Corporation at 718-383-8585.
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« Reply #55 on: August 22, 2007, 06:42:22 PM » |
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Select Red Flannel Large Breed Adult Formula Dry Dog Food 50lb Bags Voluntarily Recalled in PennsylvaniaContact: Renee Kopkowski (908) 850-7935 FOR IMMEDIATE RELEASE -- FRANKLIN, Tenn. -- August 21, 2007 -- Mars Petcare US, Inc. today announces a voluntary recall of select 50 lb bags of Red Flannel Large Breed Adult Formula dry dog food sold in two stores in Pennsylvania. Only three bags of product were actually sold, with only one bag still unaccounted for. The pet food is being recalled because it has the potential to be contaminated with Salmonella, which can cause serious infections in dogs and cats, and, if there is cross contamination, in people, especially children, the aged, and people with compromised immune systems. The recalled product should not be sold or fed to pets. Pet owners should dispose of product in a safe manner (example, a securely covered trash receptacle) and return the empty bag to the store where purchased for a full refund. Salmonella can potentially be transferred to people handling this pet food, especially if they have not thoroughly washed their hands after having contact with the product or any surfaces exposed to the product. Healthy people potentially infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers. Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Well animals can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian. Recalled pet food
Product: Red Flannel Large Breed Adult Formula dry dog food
Size: 50 pound bag
UPC Code: 4286900062
Best Buy Date: July 12, 2008
Best Buy Date Location: Back of bag
Affected Stores: The stores are located in Reedsland, PA and Richlandville, PAMars Petcare is issuing this action out of an abundance of caution and it sincerely regrets any inconvenience to pet owners as a result of this announcement. This voluntary recall has been issued because FDA detected Salmonella in a sample of Red Flannel Large Breed Adult Formula dry dog food with a best buy date of July 12, 2008 during a recent review. In an effort to prevent the transmission of Salmonella from pets to family members and care givers, the FDA recommends that everyone follow appropriate pet food handling guidelines when feeding their pets. A list of safe pet food handling tips can be found at: www.fda.gov/consumer/updates/petfoodtips080307.htmlThis product UPC has been blocked from retail sale at these locations. Additional information about the product is available on www.marspetcare.com. Pet owners who have questions about the voluntary recall should call (866) 298-8332, or visit the web site for more information.
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« Reply #56 on: August 22, 2007, 06:43:24 PM » |
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Select Krasdale Gravy Dry Dog Food 5lb Bags Voluntarily Recalled in Five States Contact: Renee Kopkowski (908) 850-7935 FOR IMMEDIATE RELEASE -- FRANKLIN, Tenn. -- August 21, 2007 -- Mars Petcare US, Inc. today announces a voluntary recall of select five pound bags of Krasdale Gravy dry dog food sold in Connecticut, Massachusetts, New Jersey, New York, and Pennsylvania. The pet food is being recalled because it has the potential to be contaminated with Salmonella, which can cause serious infections in dogs and cats, and, if there is cross contamination, in people, especially children, the aged, and people with compromised immune systems. The recalled product should not be sold or fed to pets. Pet owners should dispose of product in a safe manner (example, a securely covered trash receptacle) and return the empty bag to the store where purchased for a full refund. Salmonella can potentially be transferred to people handling this pet food, especially if they have not thoroughly washed their hands after having contact with the product or any surfaces exposed to the product. Healthy people potentially infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers. Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Well animals can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian. Recalled pet food
Product: Krasdale Gravy dry dog food
Size: 5 pound bag
UPC Code: 7513062596
Best Buy Date: July 16 & 17, 2008
Best Buy Date Location: Back of bag
Affected Stores: Various stores located in Connecticut, Massachusetts, New Jersey, New York, and Pennsylvania. Mars Petcare is issuing this action out of an abundance of caution and it sincerely regrets any inconvenience to pet owners as a result of this announcement. This voluntary recall has been issued because the FDA detected Salmonella in a sample of Krasdale Gravy dry dog food with best buy dates of July 16 & 17, 2008 during a recent review. In an effort to prevent the transmission of Salmonella from pets to family members and care givers, the FDA recommends that everyone follow appropriate pet food handling guidelines when feeding their pets. A list of safe pet food handling tips can be found at: www.fda.gov/consumer/updates/petfoodtips080307.htmlThis product UPC has been blocked from retail sale at these locations. Additional information about the product is available on www.marspetcare.com. Pet owners who have questions about the voluntary recall should call (866) 298-8332, or visit the web site for more information.
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« Reply #57 on: August 24, 2007, 01:58:24 PM » |
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Los Angeles Salad Company Voluntarily Recalls Product Because of Possible Health Risk
Contact:
John Shaughnessy
626-322-9017
FOR IMMEDIATE RELEASE -- Industry, CA -- August 22, 2007 -- Los Angeles Salad Company, located in City of Industry, CA is recalling its "Genuine Sweet Baby Carrots" with a Sell By Date Code up to and including August 16, 2007 printed on the back of the packages because the product may be contaminated with the bacteria Shigella. Shigella infection can cause diarrhea (which may be bloody), fever, nausea and vomiting. Illness usually lasts from 4 to 14 days. In some persons, especially the very young, the very old and people with compromised immune systems, the diarrhea can be more severe. Infection can occur after eating and drinking food and water that is contaminated with Shigella and can be passed from person to person.
The product was sold in packages with two labels. One is labeled "Los Angeles Salad Genuine Sweet Baby Carrots" distributed by Kroger Co. King Sooper, in Colorado, Kroger Co. Ralphs in California; Publix in Georgia, Tennessee, Alabama, South Carolina and Florida. All of these packages were sold in flexible plastic bags in 7 and 8 oz. size with a Sell By Date Code up to and including August 16, 2007. The second label was "Trader Joe's Genuine Sweet Baby Carrots" distributed by Trader Joe's in Arizona, California, New Mexico, Nevada, Oregon and Washington in 7 oz. flexible plastic bags with a Sell By Date Code up to and including August 8, 2007.
The recall was initiated after it was discovered that the same product sold in Canada was contaminated with Shigella. There were four reported incidences of illness in Canada from August 4-6, 2007. No one was hospitalized and all persons affected have fully recovered. An ongoing investigation is being conducted to find the cause of the problem, but at this time the source has not been determined.
This is precautionary notice. Consumers who have purchased Los Angeles Salad Company's "Genuine Sweet Baby Carrots" are urged to return it to the place of purchase for a full refund. Consumers with questions may contact Los Angeles Salads at (1-626-322-9017).
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« Reply #58 on: August 29, 2007, 05:20:34 PM » |
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FDA Expands Warning on Eating Raw Oysters from
Hood Canal in Washington State
Additional Growing Area Linked to Illness OutbreaksThe U.S. Food and Drug Administration is warning consumers not to eat raw oysters harvested from an additional part (growing area 5) of the southern tip of Hood Canal in Washington state due to a foodborne illness outbreak caused by Vibrio parahaemolyticus bacteria. This follows an earlier outbreak and August 10 warning about oysters harvested from growing area 6 of Hood Canal. Symptoms of the illness, vibriosis, include watery diarrhea, often with abdominal cramping, nausea, vomiting, fever, and chills. Usually these symptoms occur within 24 hours of ingestion and last no more than three days. Severe disease is rare and occurs most commonly in people with weakened immune systems. Those who believe they have experienced these symptoms after consuming raw oysters should consult their health care provider and contact their local health department. Raw oysters harvested from growing area 5 in Hood Canal from July 31 through August 20, 2007 have caused at least six people to become ill in Washington state. To date, records indicate that raw oysters from the area were distributed to Arizona, California, Colorado, Delaware, Florida, Idaho, Minnesota, New York, Oregon, Pennsylvania, Utah, Washington state, British Columbia (Canada). Bali (Indonesia), Hong Kong, Singapore, and Thailand. The Washington State Department of Health has closed the growing area associated with the illness and has asked commercial oyster harvesters and dealers who obtained oysters from this area to recall them. Consumers who have recently purchased oysters should check with the place of purchase and ask if they were harvested from the affected growing areas. The recall involves both shucked oysters and oyster in the shell (shell stock oysters). Those with weakened immune systems, including people affected by HIV/AIDS, chronic alcohol abuse, liver, stomach, or blood disorders, cancer, diabetes, or kidney disease, should avoid eating raw oysters, regardless of where they are harvested. FDA advises that consumers can continue to enjoy oysters in many cooked preparations by doing the following: At Restaurants and other Foodservice Establishments: Order oysters fully cooked. In the Shell: Purchase oysters with the shells closed Throw away any oysters with shells already opened. Never allow raw seafood to come into contact with cooked food. Boil or steam the oysters: Boil oysters until the shells open. Once shells open, boil for an additional three to five minutes. To steam—add oysters to water that is already steaming and cook live oysters until the shells open, once open steam for another four to nine minutes. Use smaller pots to boil or steam oysters. Using larger pots, or cooking too many oysters at one time, Discard any oysters that do not open during cooking. Shucked Oysters: Never allow raw seafood to come into contact with cooked food. Cook the oysters in one of the following ways: Boil or simmer shucked oysters for at least three minutes or until the edges curl. \ Fry at 375° F for at least three minutes. Broil three inches from heat for three minutes. Bake at 450° F for 10 minutes. For more information: Hood canal oyster area closed — second closure due to illness outbreak www.doh.wa.gov/Publicat/2007_news/07-143.htm
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« Reply #59 on: August 29, 2007, 05:22:06 PM » |
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Bella Cucina Issues Allergy Alert on Undeclared Walnuts in Death by Chocolate Cookies
Contact:
Bella Cucina
678-539-8400
FOR IMMEDIATE RELEASE -- Atlanta, GA -- August 27, 2007 -- Bella Cucina of Atlanta, Georgia is recalling units of Death by Chocolate cookies if your bag does not correctly state that the product contains walnuts. People who have an allergy or severe sensitivity to Walnuts run the risk of serious or life threatening allergic reaction if they consume these products.
Death by Chocolate cookies may have been sold directly to consumers in the following retail stores:
Store
Contact Information
Ballins, LTD
Wendy Legarde
550 Elmwood Park Blvd
Suite B
Harahan, LA 70123
At Home Store
At Home Store
Rosie Witherspoon
52 N. Main St
Fairfield, IA 52556
Perfect Package
Perfect Package
Attn:Robin
263 Park Ave
Worcester, MA 1609
USA
Lincoln Finishing Touches-NE
Lincoln Finishing Touches-NE
Attn: Linda Spurrier
3945 S. 48t
Lincoln, NE 68506
USA
Farm Fresh To You Store
Farm Fresh To You Store
Freeman O Barsotti
1 Ferry Building
Shop 9
San Francisco, CA 94105
The Fig Pantry
The Fig Pantry (bill)
Attn: Jennifer
21800 Schellville Rd
Suite C
Sonoma, CA 95476
USA
Black Salt
Black Salt
c/o:Scott Weinstein-Fish Marke
4883 MacArthur Blvd NW
Washington, DC 20007
Great American
Great American
Attn: Amy Hamilton-Hails
4121 16th Street N.
St Petersberg, FL 33703
Kiawah Island Resort
Osprey Point
Attn: Ashley Agapion Magee
700 Governors Dr.
Kiawah Island, SC 29455
Trapp & Co
Trapp & Co.
Attn: Helga/Steven
4110 Main Street
Kansas City, MO 64111
US
Joli Home and Events
Joli Home & Events
Cheryl Hunter
8B Market
Beaufort, SC 29906
James Welch
James Welch
James Welch
260 Balfour Drive
Winter Park, FL 32792
Crabby Chic
Crabby Chic
Attn: Pam Teebo
4407 Cascade Rd
Wilmington, NC 28409
McArdles Forest and Garden Center
McArdle's Forest & Garden Ctr
Attn :Sari
48 Arch Street
Greenwich, CT 6830
BCAF Grand Central Station
Bella Cucina Artful Food - GCS
1870 Murphy Avenue
Atlanta, GA 30310
Wines of Distinction, Inc.
Wines of Distinction, Inc.
Attn: Katherine Rose
230 E Main St
Abingdon, VA 24210
USA
Domaine Carneros
Domaine Carneros
Attn:Rose
1240 Duhig Road
Napa, CA 94559
Build a Basket
Build A Basket
Attn: Mena F/Scott Maybaum
32 Rte 10 West
East Hanover, NJ 07936
USA
Design Line Interiors
Design Line Interiors
Attn:Connie
4863 Shawline Street
Ste. E
San Diego, CA 92111
USA
BCAF Virginia Highlands
BCAF-Virginia Highlands
1050 North Highland Avenue
Atlanta, GA 30306
Nest
Nest
Attn: Mary Matheson
4699 South Hollady Blvd
Salt Lake City, UT 84117
Counrty Store - CA
Country Store -CA
Attn:Carol L Holmes
2408 W. Adrian Street
Newberry, CA 91320
Graeagle Gift Shop
NO CONTACT
Moravian Florist
Moravian Florist
Attn: Sue Kirchhoffer
2286 Richmond Rd.
Staten Island, NY 10306
USA
The Cheshire Cat
The Cheshire Cat
Scott Comstock
34121 N. Rt 45
Grayslake, IL 60030
Kimball Shop
Kimball Shop
Nancey Kimball
135 Main St. NE
Harbor,ME 04662
USA
Sayville General Store Inc
Sayville General Store, Inc
Attn: Jackie
44 Main Street
Sayville, NY 11782
Chintz & Company
Chintz & Company
Attn: Nicole de Goutiere
1720 Store St
Victoria, BC V8W 1V5
Canada
English Green Interiors
English Green Interiors
Attn: Deborah Green
P. O BOx 2541
Cashiers, NC 28717
Bella Donna Designs
Bella Donna Designs
Attn:Donna
131 Hurst Cir
Franklin, NC 28734
Equipment Di Vin
Equipment Di Vin
Cheryl Webster
1412 Larimer Street
Denver, CO 80202
Celebrations - FL
Celebrations-FL
Attn: Debbie
717 N. 12th Ave.
Pensacola, FL 32501
French's Kitchen & Bath
French's Kitchen & Bath
202 5th St
Hollister, CA 95023
USA
Fanciful Gift Baskets
Fanciful Gift Baskets
Attn: Dave
5617 Melrose
Los Angeles, CA 90038
Harris & Clark General Store
Harris & Clark General Store
Anissa Harris
2539 Knox St
Atlanta, Georgia 30317
Breckenridge Cheese and Chocolate
Breckenridge Cheese & Chocolate
Attn: Anne
P.O. Box 3771
Breckenridge, CO 80424
USA
Son of Moon Fine Foods
Son of the Moon
Eva Bunnell
346 South Main St.
Middletown, CT 06457
USA
Roche Bros Supermarket
Roche Bros. #101
165 Linden Street
Wellesley Hill, MA 02481
Tenzie & Co
Tenzie & Co.
1116-A Coolidge Street
Lafayette, LA 70503
USA
Pine Away
Pine Away
216 Main St.
Annapolis, MD 21401
USA
Bee Entertaining
Bee Entertaining
124 S. Webster St
Naperville, IL 60540
USA
The country Farmer
The Country Farmer
1 Bloomer Rd
N. Salem, NY 10560
All stores have been notified of the incident.
The Death by Chocolate cookies is bags are in a 6oz. bag with a sleeve label. The UPC code for this product is 19193 00020. These cookies have a three month shelf life. The cookies being recalled were made on June 14, 2007 and also July 5, 2007 for a total of 36 cases, 12 units per case. The cookie ingredient list did not contain Walnuts.
No Illness have been reported to date.
Consumers should contact Bella Cucina directly at 678.539.8400 so we can refund or replace the cookie bag.
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« Reply #60 on: August 29, 2007, 05:23:12 PM » |
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Metz Fresh Announces Voluntary Recall of Spinach
Contact:
Metz Fresh
831-386-1018
FOR IMMEDIATE RELEASE -- Salinas, CA -- August 28, 2007 -- Metz Fresh, LLC is voluntarily recalling bagged spinach as a result of a positive test for Salmonella found during routine company testing.
The spinach is distributed under the label Metz Fresh, in both retail and food service packages. These include 10 and 16 oz bags as well as 4-2.5 lb. and 4 lb. cartons. The only Metz Fresh product affected is spinach that bears the tracking codes 12208114, 12208214 and 12208314. It was distributed in the continental United States and Canada.
There have been no reports of illness or problems related to this spinach.
Salmonella is a common food borne pathogen that can cause severe illnesses, including fever, abdominal cramps and diarrhea. While most individuals recover in three to five days without medical intervention, the infection can be life-threatening to young children, the elderly and those with compromised immune systems. Consumers with any of these symptoms should call their physician.
Consumers are advised to discard this product or return it to the place of purchase for a refund. Consumers with questions about the recall should contact 831-386-1018.
"Nothing is more important to Metz Fresh than the safety of our consumers, period," said Andrew Cumming, President of Metz Fresh. "As soon as we learned of the presumptive positive test, we directed all customers to hold all boxes of the spinach affected as a precaution. Now, with this positive test confirmation, there is no question that we would recall and destroy all spinach bearing these three codes."
The positive test came during independent lab testing Metz Fresh conducts on all of its products. Through its labeling and numbering system, Metz Fresh has already tracked, located and put 'holds' on the vast majority of the cartons of spinach affected. That spinach will not be released into the marketplace.
While the positive test came from only one sample of many on three packing lines, Metz Fresh has, as a precaution, chosen to recall all of the spinach from the ‘field lot’ packed that day on all three lines.
Metz Fresh is keeping appropriate authorities updated on the status of the voluntary recall.
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« Reply #61 on: August 31, 2007, 09:44:17 AM » |
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Stirrings LLC Participates in Voluntary Nationwide Recall of Rimmer® Brand Mojito Cocktail Garnish Due to Possible Health Risk from Contaminated Raw Ingredient Supplied by Van de Vries Spice Corporation
Contact:
Paul Nardone
508-324-9800
FOR IMMEDIATE RELEASE -- Stirrings LLC, of Fall River, Massachusetts is recalling its 3.5 oz packages of Rimmer® Brand Mojito Cocktail Garnish (UPC# 80999 00046) with the best by codes 10/27/08, 10/30/08, 11/23/08, 12/01/08, 12/04/08 and 01/03/09 printed on the side of the tin. The recall may involve approximately 5,000 cases of its Rimmer® Brand Mojito Cocktail Garnish supplied by Van de Vries Spice Corporation (formerly Atlantic Quality Spice) of Edison, NJ because they have the potential to be contaminated with Salmonella. Although Stirrings LLC's tests of finished product samples were negative for the presence of Salmonella, parsley powder, one of several ingredients supplied by Van de Vries Spice, tested positive for Salmonella.
The presence of Salmonella can cause serious and sometimes fatal infections in young children, frail, or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more serious illnesses such as arterial infections (i.e. infected aneurysms), endocarditis and arthritis.
Rimmer® Brand Mojito Cocktail Garnish was distributed nationwide through distributors, retail stores, internet sales and cocktail establishments.
Immediately after Van de Vries brought to Stirrings attention that a parsley powder used in a single lot of Mojito Rimmer product potentially could contain Salmonella based on FDA testing, Stirrings retained expert laboratories, primarily Shuster Laboratories of Canton, Massachusetts to test samples of its Mojito Rimmer product for Salmonella. Testing of 24 samples drawn from the Van de Vries lot of Mojito Rimmer failed to reveal the presence of Salmonella in the Mojito Rimmer product.
No illnesses have been reported to date.
Stirrings CEO Paul Nardone explained, "We have removed parsley powder from our Rimmer Cocktail Garnish formula. This ingredient represents less than one half of one percent of the blend and was used primarily as a natural colorant." Nardone further stated, "We have initiated a recall as a precaution and assurance to our customers that we stand behind our product quality 100%."
Consumers who have purchased Rimmer® Brand Mojito Cocktail Garnish with the best by codes noted above are asked to return it to the place of purchase for a full refund. Consumers with questions may contact the Company toll-free at 866-648-8239.
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« Reply #62 on: August 31, 2007, 09:45:12 AM » |
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Everlasting Distributors, Inc. Recalls Blue Ocean Smoked Indian Sardine Tamban Because of Possible Health Risk
Contact:
Richard Ng
201-823-0800
FOR IMMEDIATE RELEASE -- Bayonne, NJ -- August 29, 2007 -- Everlasting Distributors, Inc. of Bayonne, NJ, is recalling its Blue Ocean Smoked Indian Sardine Tamban 8oz. packaged frozen products because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Botulism, a potentially fatal form of food poisoning, can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention.
Blue Ocean Smoked Indian Sardine Tamban was distributed in New York and New Jersey areas and it reached consumers through retail stores.
Blue Ocean Indian Sardine Tamban comes in an uncoded white styropor foam tray and vacuum packed with a clear plastic bag.
The potential for contamination was noted after routing testing.
No illnesses have been reported to date in connection with this problem.
Consumers who have purchased the Blue Ocean Smoked Indian Sardine Tamban 8oz. frozen product are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Everlasting Distributors, Inc. at (201) 823-0800.
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« Reply #63 on: September 01, 2007, 04:25:27 AM » |
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American Pie Recalls Marie Callender Turtle Pies Because of a Possible Health Risk
Contact:
American Pie, LLC
1-888-339-7437, x3987
FOR IMMEDIATE RELEASE -- Woodbury, NY -- August 25, 2007 -- American Pie, LLC, Woodbury, NY, is voluntarily recalling 1440 cases of its Marie Callender Turtle Pies with date codes 07 (from military time 11:45 up to and including 16:00) 143 because the product was inadvertently shipped prior to the company obtaining satisfactory microbial test results. No specific pathogens were found. The recall is being conducted as a precautionary measure. Consumption of this product may lead to gastrointestinal illness, nausea, or vomiting.
The product was shipped to the following locations:
Kroger Supermarkets: Columbus, OH; Houston, TX; Roanoke, VA; Dallas, TX; Atlanta, GA; Memphis, TN; Shelbyville, TN; Louisville, KY;
Giant Eagle Supermarkets: Akron, Canton, Lake, Cleveland, Columbus, Erie, Toledo, Johnston (all in Ohio); also New Castle, MD; Pittsburgh, PA; and Youngstown, WV;
Hy-Vee Supermarkets: Iowa, Illinois, Kansas, Minnesota, Maryland, Nebraska, and South Dakota.
There was no direct foreign distribution.
The pies are packaged in 28oz. boxes with UPC code 12781 10280.
The recall was initiated after it was discovered that the product had been distributed without company authorization.
No illnesses have been reported to date in connection with this situation.
Consumers who have purchased Marie Callender Turtle Pies with the above date codes are urged to return them to the place of purchase. Consumers with questions may contact the company at 1-888-339-7437, x3987.
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« Reply #64 on: September 07, 2007, 05:27:10 PM » |
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Bodee LLC, Inc. Issues A Voluntary Nationwide Recall of All Zencore Tabs, a Product Marketed as a Dietary Supplement Contact: Bodee LLC help@zencoretabs.comFOR IMMEDIATE RELEASE -- Century City, CA – August 31- Bodee LLC, 2222 Avenue of the Stars, 702E, Century City, CA 90067, announced today that it is conducting a voluntary nationwide recall of all the company's supplement product sold under the name Zencore Tabs. Bodee LLC is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of Zencore Tabs samples found the product contains potentially harmful, undeclared ingredients. FDA asserts that its chemical analysis revealed that one lot of Zencore Tabs contains aminotadalafil, an analog of tadalafil, the active ingredient of a FDA-approved drug used for Erectile Dysfunction (ED). FDA maintains Aminotadalafil is close in structure to tadalafil and is expected to possess a similar pharmacological and adverse event profile. Further, FDA declares another lot of Zencore Tabs contains sildenafil, the active ingredient of another FDA-approved drug used for ED, as well as sulfosildenafil and sulfohomosildenafil, both are analogs of sildenafil. All of these undeclared chemicals pose a threat to consumers because they may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. ED is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance. Zencore Tabs is sold in health food stores and by mail order nationwide and in Canada. The Zencore Tabs product is sold as a 2-capsule blister pack packaged in a retail booklet with five booklets in a box. Customers who have this product in their possession should stop using it immediately and contact their physician if they have experienced any problems that may be related to taking this product. Any adverse events that may be related to the use of this product should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088 or by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787. The company advises that any unused portion be returned to Bodee LLC for a full purchase price refund by calling (800) 935-0296 for instructions on the return and refund process. The Company is taking this voluntary action because it is committed and is always concerned with the health of persons who have consumed this product. The Company is reviewing the procedures and policies of all firms involved with the manufacture of the product to ensure that there will be no future issues with regard to Zencore Tabs’ composition. The Company is working closely with the FDA in the recall process and is committed to the quality and integrity of its products. It sincerely regrets any inconvenience to consumers and its other customers.
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« Reply #65 on: September 10, 2007, 04:47:11 PM » |
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Urgent: Abbott Notifies Users of Precision Xtra™, Optium™, ReliOn® Ultima, Rite Aid® and Kroger® Blood Glucose Meters to Check Display Screens Contact: Tama Antonia Donaldson (510) 749-5449 FOR IMMEDIATE RELEASE -- Alameda, CA -- August 31, 2007 -- Abbott is initiating a worldwide medical device correction for users of its Precision Xtra™, Optium™, ReliOn® Ultima, Rite Aid® and Kroger® blood glucose meters manufactured after January 31, 2007. If the meter is dropped on a hard surface, part or all of the display screen may not work properly or may appear blank, which could result in an inability to view blood glucose test results. The inability to generate blood glucose results could result in significant risk for hypoglycemia or hyperglycemia. Users of these meters who note that the display screen is not working properly should immediately stop using their meter as referenced in the User Guide and call Abbott Diabetes Care customer care for assistance at 1-877-844-4404. Through internal testing, Abbott Diabetes Care has found that when recently produced meters are dropped onto a hard surface, part of the display can be jarred or disconnected, thereby making it difficult to read the lot number or date information, or causing the screen to appear blank. No injuries have been reported to date. Patients should keep their glucose meters in the wallet provided to offer additional protection for the meter. If the meter is dropped on a hard surface, patients should immediately perform a meter display check. Instructions on how to do this are detailed in the meter’s Users Guide. If no problems are encountered during the automatic display check, the meter is ready for use. Customers may call Abbott Diabetes Care customer care at 1-877-844-4404 to determine the date their meter was manufactured. Customers may also call customer care if they have questions or need a replacement meter. Precision Xtra™, Optium, ReliOn® Ultima, Rite Aid® and Kroger® blood glucose meters have been distributed via retail and mail order pharmacies, physician offices and distributors. Abbott is notifying physicians, pharmacists, distributors and registered users by letter. Blood glucose test strips used with these meters are not affected by this notification. More information about this notification is available on the company’s website, www.abbottdiabetescare.com.
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« Reply #66 on: September 10, 2007, 04:48:58 PM » |
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Listeria Detected in Organic Pastures Raw Cream
CDFA Issues Order to Withdraw Product; No Illnesses Reported
Contact:
Steve Lyle
916-654-0462
FOR IMMEDIATE RELEASE -- Sacramento, CA -- September 7, 2007 -- The California Department of Food and Agriculture has issued an order to Organic Pastures Dairy Company to withdraw from retail distribution Grade A raw cream manufactured at their facility in Fresno, due to detection of Listeria monocytogenes bacteria.
Under the recall, Organic Pastures brand Grade A raw cream with code dates SEP 14 through SEP 21 is to be pulled immediately from retail shelves and consumers are strongly urged to dispose of any product remaining in their refrigerators. Until further notice, Organic Pastures may not produce raw cream for the retail market.
The quarantine order came following laboratory confirmation of Listeria monocytogenes bacteria. CDFA inspectors found the bacteria as a result of product testing conducted as part of routine inspection and sample collection at the facility.
The withdrawal order involves removal of raw cream from grocery stores, retail outlets and farmers markets throughout California.
The great majority of cream consumed in California is pasteurized. Raw cream is not. Pasteurization eliminates the risk of bacterial illness.
Listeria monocytogenes may cause listeriosis among "at risk" people, including pregnant women, newborns, older adults, and people with weakened immune systems. Symptoms include fever, muscle aches, and sometimes nausea or diarrhea. If infection spreads to the nervous system, symptoms such as headache and stiff neck can occur. Infected pregnant women may experience only a mild, flu-like illness; however, infections during pregnancy can lead to more serious problems for the fetus. Consumers should seek immediate medical care if they develop these symptoms.
Consumers should discard the raw cream or return it to the place of purchase for a refund. California consumers who have purchased Organic Pastures brand raw cream may call the company at 559- 352-6585 with questions about the product withdrawal.
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« Reply #67 on: September 10, 2007, 08:01:04 PM » |
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Jensen's Old Fashioned Smokehouse Inc. Recalls Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion, and PCC brand Smoked Salmon Spread Because of Possible Health Risk
Contact:
Mike Jensen
206-669-7590
FOR IMMEDIATE RELEASE -- Seattle, WA -- September 7, 2007 -- Jensen's Old Fashioned Smokehouse Inc. of Seattle, WA is recalling 480 tubs of Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion and 132 tubs of PCC brand Smoked Salmon Spread all–natural, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion, and PCC brand Smoked Salmon Spread all – natural were distributed in retail stores in Western Washington.
Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion is coded Sell By 10/14/07 and 10/15/07, and PCC brand Smoked Salmon Spread all–natural is coded Sell By 9/29/07. Both products were sold in 7 oz. plastic tubs.
No illnesses have been CONFIRMED to date. The recall was the result of a routine sampling program by the company which revealed that the finished products contained the bacteria.
Consumers who have purchased Jensen's Seattle Style Wild Smoked Salmon Spread Lemon Dill and Onion, and PCC brand Smoked Salmon Spread all – natural are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the Quality Assurance Department at Jensen's Smokehouse at 206-364-5569.
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« Reply #68 on: September 11, 2007, 04:46:25 AM » |
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« Reply #69 on: September 13, 2007, 04:59:03 PM » |
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Yuck...sushi of any kind would make me ill. :crazytongue:Anyhow...at least Aquastar is refunding your money. As for Wal-Mart, I am really not the one to ask here. I like Wal-Mart, and don't wish to demean the company...unless warranted. I myself would not pursue anything with Wal-Mart. I'm sure that Wal-Mart just made a mistake in not pulling the product sooner. If anything, I would pursue Aquastar, especially if my illness resulted in medical bills and such. But there are getting to be so many bad-food recalls, that it is harder and harder to keep up with what is bad and what is not...what has been recalled and what has not, etc. |
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« Reply #70 on: September 13, 2007, 05:00:15 PM » |
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Strong America Limited Issues Alert on Undeclared Sulfites in Great Wall Brand Chinese Wolfberry
Contact:
Mr. Yang
(718) 628-6200
FOR IMMEDIATE RELEASE -- Long Island City, NY -- September 10, 2007 -- Strong America Ltd. of Long Island City, NY is recalling Chinese Wolfberry, because it may contain undeclared sulfites. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume this product.
The recalled Great Wall brand Chinese Wolfberry is packed in uncoded 7oz packages and were sold in GA, NY, and TN.
No illnesses have been reported to date.
The recall was initiated after routine sampling by the New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by the Department’s Food Laboratory personnel revealed the presence of sulfites in the product, which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics; Anaphylactic shock could occur in certain sulfites sensitive individuals upon ingesting 10 milligrams or more of sulfites. Analysis of the Chinese Wolfberry revealed that it contained 12.87 milligrams per serving.
Consumers who have Great Wall brand Chinese Wolfberry can return the product to the place of purchase for a full refund. Consumers with questions may contact the company at 718-628-6200
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« Reply #71 on: September 13, 2007, 05:01:40 PM » |
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Harry & David Recalls Harry and David Hearthside Soups, Southwestern Chicken Chili Mix for an Undeclared Milk Ingredient
Contact:
Bill Ihle
541-864-2145
FOR IMMEDIATE RELEASE -- Medford, OR -- September 12, 2007 -- Harry & David Operations Corp., of Medford, Oregon, is recalling approximately 1440 bags of Harry and David Hearthside Soups, Southwestern Chicken Chili Mix, because they may actually contain another chili soup mix, and thus contain a milk ingredient (whey), not declared in the ingredient statement.
People who have an allergy or severe sensitivity to dairy products run the risk of serious or life-threatening allergic reaction if they consume these products.
Harry & David is recalling all Harry and David Hearthside Soups, Southwestern Chicken Chili Mix with a 8221-1 lot code. These products include: Clear plastic bags of soup mix, 12 to 16 oz. in weight, tied at the top with a cream and red colored ribbon. The lot code can be found on the price sticker on the bottom of the bag. Please note that the price sticker states "Fajita Chili". This product was made for Harry & David by Conifer Specialty, Inc., a co-packer.
These products were distributed throughout the United States through Harry and David Stores beginning March 5th, 2007.
There have been no reported illnesses associated with this product to date. Anyone concerned about an illness associated with this product should contact a physician immediately.
This problem occurred when bags labeled for a previous run of Southwestern Chicken Chili Mix were inadvertently used for a subsequent run of a different product, Fajita Chili Mix. The Fajita Chili Mix contains a milk ingredient not declared on the Southwestern Chicken Chili Mix ingredient statement. The problem will be prevented in the future by assuring that the production line is cleared of labeled bags during product change over.
Consumers with questions about the recalled product may phone the Customer Service division at 800-345-5655, 24 hours a day. Customers may arrange for refunds through this number as well.
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« Reply #72 on: September 15, 2007, 03:39:48 PM » |
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B. Braun Medical Inc. Issues Nationwide Recall of Normal Saline Flush Syringes with Lot Numbers Ending in "SFR" Contact: B. Braun Medical Inc. (800) 227-2862 FOR IMMEDIATE RELEASE -- September 14, 2007 – B. Braun Medical Inc., Bethlehem, PA, announced on July 30, 2007 a voluntary nationwide recall of Normal Saline Flush syringes with lot numbers ending in "SFR" due to an increase in customer complaints for particulate matter in the saline. The FDA has been apprised of this action. The introduction of particulate matter into the blood stream may result in phlebitis and / or damage to vital organs such as the brain, kidneys, heart and lungs. To a less likely extent, there is a potential for the development of pulmonary embolism or silicone embolism syndrome, which could cause severe injury and / or death. Symptoms would generally be expected to develop quickly and are unlikely to develop more than 24 - 48 hours after the administration of the product. However, the risk associated with use of this product is cumulative and increases with each additional exposure. A patient may not develop any symptoms until they have received multiple doses of the product. To date, B. Braun has received no reports of any patient injury associated with this issue. Customers that have the recalled product in their possession should discontinue use immediately and contact their physician if they have experienced any problems that may be related to usage of this product. Customers that have the affected product in their possession may contact the B. Braun Medical Inc. Customer Support Department at (800) 227-2862, Monday through Friday, 8 AM to 7 PM EST for instructions for handling the affected product and to arrange for replacement product. This voluntary recall affects normal saline 3mL in 12mL syringes, designated by product code 513584, and normal saline 10mL in 12mL syringes, designated by product code 513587. Between June 11 and July 18 of this year, B. Braun Medical Inc. distributed approximately 33,000 units of product code 513584 and 1.2 million units of product code 513587 of lot numbers ending in "SFR" to hospitals and distributors. The product code, identified as REF, and lot number, identified as LOT, can be found on the syringe label just below the product description. These flush syringes have been found to contain particulate matter, which has been identified as a medical grade silicone. While this silicone is biocompatible, routinely used in the medical device industry and is an expected component of these syringes, the visible particulate matter caused by the silicone in these "SFR" lots may pose a health risk. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Online: www.fda.gov/medwatch/report.htm Regular Mail: use postage-paid FDA form 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to MedWatch 5600 Fishers Lane, Rockville, MD 20852-9787 Fax: 1-800-FDA-0178
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« Reply #73 on: September 18, 2007, 04:16:40 PM » |
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Dole Fresh Vegetables Announces Voluntary Recall of 'Dole Hearts Delight' Packaged Salads
Contact:
Marty Ordman
1-818-874-4834
FOR IMMEDIATE RELEASE --Monterey, Calif. -- Sept. 17, 2007 --- Dole Fresh Vegetables, a division of Dole Food Company, Inc., today announced that it is voluntarily recalling all salad bearing the label "Dole Hearts Delight" sold in the U.S. and Canada with a "best if used by (BIUB)" date of September 19, 2007, and a production code of "A24924A" or "A24924B" stamped on the package. The "best if use by (BIUB)" code date can be located in the upper right hand corner of the front of the bag. The salad was sold in plastic bags of 227 grams in Canada and one-half pound in the U.S., with UPC code 071430-01038.
Symptoms of E. coli O157:H7 exposure could include stomach cramps and diarrhea. Bloody diarrhea may develop. E. coli disease sometimes leads to a complication called hemolytic uremic syndrome (HUS). If you exhibited any of these symptoms within 3 to 5 days of consuming any of the products specified above, seek medical attention.
To date, Dole has received no reports that anyone has become sick from eating these products. The recall is occurring because a sample in a grocery store in Canada was found through random screening to contain E. coli O157:H7. No other Dole salad products are involved.
Eric Schwartz, President, Dole Fresh Vegetables, stated: "Our overriding concern is for consumer safety. We are working closely with the U.S. Food and Drug Administration, the Canadian Food Inspection Agency, and several U.S. state health departments."
Consumers who may still have any of the "Dole Hearts Delight" salads with a "best if used by date" of September 19 and a production code of "A24924A" or "A24924B" should dispose of the product. This product was sold in Ontario, Quebec and the Maritime Provinces in Canada and in Illinois, Indiana, Maine, Michigan, Mississippi, New York, Ohio, Pennsylvania, Tennessee and neighboring states in the U.S. Consumers can call the Dole Consumer Center toll-free at 800-356-3111. Consumers are reminded that products should not be consumed after the "best if used by" date.
Dole Food Company, Inc., with 2006 revenues of $6.2 billion, is the world's largest producer and marketer of high-quality fresh fruit, fresh vegetables and fresh-cut flowers. Dole markets a growing line of packaged and frozen foods and is a produce industry leader in nutrition education and research.
This release contains "forward-looking statements," within the meaning of the Private Securities Litigation Reform Act of 1995 that involve a number of risks and uncertainties. Forward looking statements, which are based on management's current expectations, are generally identifiable by the use of terms such as "may," "will," "expects," "believes," "intends" and similar expressions. The potential risks and uncertainties that could cause actual results to differ materially from those expressed or implied herein include weather-related phenomena; market responses to industry volume pressures; product and raw materials supplies and pricing; changes in interest and currency exchange rates; economic crises and security risks in developing countries; international conflict; and quotas, tariffs and other governmental actions. Further information on the factors that could affect Dole's financial results is included in its SEC filings, including its Annual Report on Form 10-K.
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« Reply #74 on: September 19, 2007, 06:58:50 PM » |
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Bravo! Issues Nationwide Recall of Select Poultry Products for Dogs and Cats Contact: David Bogner (866) 922-9222 FOR IMMEDIATE RELEASE --Vernon, CT -- Sept. 18, 2007--- Bravo! announces a voluntary recall of select tubes of three of its poultry products for cats and dogs. The pet food is being recalled because two of the products have the potential to be contaminated with Salmonella and Listeria monocytogenes, while the other product has the potential to be contaminated with Listeria monocytogenes. Both Salmonella and Listeria are organisms which can cause serious infections in dogs and cats, and if there is cross contamination, in people, especially small children, frail or elderly people, and others with weakened immune systems. Healthy people with Salmonella infection may only suffer short-term symptoms, such as high fever, severe headache, vomiting, nausea, abdominal pain, and diarrhea. Long term complications can include arthritis and other more serious ailments. Healthy people with Listeria infection may only suffer short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea. Listeria infection can cause miscarriages and stillbirths among pregnant women. The company has received no reports of illness in either people or animals associated with any of the three products. The recalled products are distributed nationwide to distributors, retail stores, internet sales and directly to consumers, and they can be identified by the batch ID code located on the hang tag attached to the bottom of the plastic film tubes. The recalled products should not be sold or fed to pets. Pet owners should return unopened frozen tubes of food to the store where purchased for a full refund. Pet owners should dispose of opened tubes of product in a safe manner (example, a securely covered trash receptacle) and return the washed plastic batch ID tag to the store where purchased for a full refund. Recalled Pet Food
Product: Bravo Original Formula Chicken Blend frozen raw food
Product Numbers: 21-102, 21-105, 21-110
Sizes: 2 pound, 5 pound and 10 pound tubes
Batch ID code (on hang tag): 236
Reason for Recall: Salmonella, Listeria
Product: Bravo Original Formula Turkey Blend frozen raw food
Product Numbers: 31-102, 31-105, 31-110
Sizes: 2 pound, 5 pound and 10 pound tubes
Batch ID code (on hang tag): 236
Reason for Recall: Listeria
Product: Bravo Basic Formula Finely Ground Chicken frozen raw food
Product Number: 21-212
Size: 2 pound tube
Batch ID Code (on hang tag): 226
Reason for Recall: Salmonella, ListeriaOther Batch IDs for these same products are not involved in the recall. Bravo! is issuing this action out of an abundance of caution and sincerely regrets any inconvenience to pet owners as a result of this announcement. This voluntary recall has been issued because the FDA detected the bacteria in samples during a recent review. In an effort to prevent the transmission of Salmonella from pets to family members and care givers, the FDA recommends that everyone follow appropriate pet food handling guidelines when feeding their pets. A list of safe pet food handling tips can be found at: http://www.fda.gov/cvm/CVM_Updates/foodbornetips.htm. People may risk Salmonella infection not only by handling these pet foods, but also by contact with pets or other surfaces exposed to these foods, so it is important that they thoroughly wash their hands with hot water and soap. Anyone who is experiencing the symptoms of Salmonella or Listeria infection after having handled the recalled product should seek medical attention. Consumers may report any complaints to FDA's local District Complaint Coordinator’s located on the FDA website: http://www.fda.gov/opacom/backgrounders/complain.html. Healthy cats and dogs rarely become sick from Salmonella. Animals ill with Salmonella will display symptoms similar to the ones listed above for humans. People who have concerns about whether their pet has Salmonella or not should contact their veterinarian. For more information on the Bravo recall, please visit www.bravorawdiet.com, or call toll free (866) 922-9222
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