Fine Land Corp Issues Alert on Undeclared Sulfites in Golden Girl Brand "Mut Gung" Sweetened Ginger

Contact:
Mainy Chen
917-939-5595

FOR IMMEDIATE RELEASE --Brooklyn, NY -- April 8, 2008 --- Fine Land Corp, 239 Bay 20th Street, Brooklyn, NY 11214 is recalling its Golden Girl brand "Mut Gung" sweetened ginger because it contains undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.

The recalled Golden Girl brand "Mut Gung" sweetened ginger comes in a 7 ounce, uncoded rigid plastic container. The product was distributed nationwide. It is a product of Vietnam

The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of undeclared sulfites in Golden Girl brand "Mut Gung" sweetened ginger which did not declare sulfites 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 sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.

No illnesses have been reported to date in connection with this product. Consumers who have purchased Golden Girl brand "Mut Gung" sweetened ginger should return the packages to the place of purchase for a full refund. Consumers with questions may contact the company at 718-714-1850.

Allergy Alert on Undeclared Dairy in 11-Ounce Single Serve Silk Soymilk Chocolate Flavor in Plastic Bottles

Contact:
Marguerite Copel
(214) 721-1273

FOR IMMEDIATE RELEASE --Mount Crawford, Virginia -- April 23, 2008 --- WhiteWave Foods Company is voluntarily recalling 11-ounce plastic single serve bottles of Silk Soymilk Chocolate Flavor because it may contain undeclared milk protein. The individual bottles are printed with both a "use by" date of May 7, 2008 (printed as 05 07 08) and a Universal Product Code (UPC) of 2529360028. Consumers can find this information on the back of the individual bottle.
People who have an allergy or severe sensitivity to milk protein run the risk of a health problem or illness if they consume this product. Some reactions have been reported.

This affected product was distributed nationwide and reached consumers through retail and foodservice outlets. WhiteWave's sales team is working with distributors to actively recover any affected product remaining on store shelves.

HOW TO IDENTIFY THE RECALLED PRODUCT

This recall includes only 11-ounce single serve plastic bottles of Silk Soymilk Chocolate Flavor with both a "use by" date of May 7, 2008 (printed as 05 07 08) and a UPC code of 2529360028. Consumers should look for this information on the back of the bottle.

The Company apologizes for any inconvenience to its customers. Consumers who purchased the product may return it to the place of purchase for a full refund or exchange. Consumers with questions can contact the Company at 1-800-587-2259.

The Food and Drug Administration has been notified of this recall.

Updated Press Release: Lezza Blue Raspberry Italian Ice Recalled

Contact:
Cedar Crest Specialties, Inc.
1-866-233-2788

FOR IMMEDIATE RELEASE -- May 6, 2008 -- Cedar Crest Specialties, Inc., Manitowoc, Wisconsin announced on Friday, May 2nd 2008 a recall on one lot code of Lezza Blue Raspberry Italian Ice because, it may contain milk allergen protein that is not listed in the product’s ingredient statement. People who have an allergy or severe sensitivity to milk may experience a potentially serious or life-threatening allergic reaction if they consume this product.

The product is in round plastic pint containers with a lot code of 2116. Blue Raspberry is the flavor of the product.

The product was distributed to retail outlets in Illinois, Wisconsin, Oklahoma, Texas, Michigan, Louisiana, Kansas, Indiana, Georgia, Florida, Ohio, Missouri, Kentucky, Nebraska, Pennsylvania, Arkansas, and Minnesota during 2006 and 2007.

There is no health risk for consumers who are not allergic to milk.

No other Lezza Italian Ice products are included in this recall. The product is flavored frozen water ice and must be kept frozen.

There is one reported allergic reaction attributed to this product. After customer reported allergic reaction, product in customer’s possession was retrieved and sent to independent lab for analysis. Unopened product was also sent to independent lab for testing. Decision for recall was reached after lab tests were completed. Only one complaint was filed about lot code 2116.

Concerned consumers are encouraged to return any affected product

Sweetwater Valley Farm, Inc. Recalls Tennessee Aged Black Pepper Cheese

Contact:
John Harrison
Sweetwater Valley Farm, Inc.
877-862-4332

FOR IMMEDIATE RELEASE -- May 15, 2008 -- Sweetwater Valley Farm, Inc. of Philadelphia, TN is recalling Tennessee Aged Black Pepper Cheese 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.

Tennessee Aged Black Pepper Cheese, Lot Number 616-361 was distributed in 5, 7, and 10 ounce bars through our retail store in Philadelphia, TN and a Winery in Portland, TN. 

Less than 100 pounds was distributed.

This product was distributed between December 27, 2007 and May 12, 2008.

No illnesses have been reported.

The recall was the result of a routine sampling program by the Tennessee Department of Agriculture which revealed that the finished product contained the bacteria. The company has ceased the distribution of this lot as the company continues their investigation as to what caused the problem.

Consumers who have purchased lot number 616-361 of this product are urged bring it to the store for replacement or refund or ship it back to the store for replacement or refund.  Contact the company’s consumer affairs department at 1-877-862-4332 for further information.

Orval Kent Foods Recalls Single Limited Production Run of Amish Macaroni Salad Sold Under the Orval Kent and Yoder’s Brand Names

Contact:
Orval Kent
1-800-544-1246

FOR IMMEDIATE RELEASE -- May 28, 2008 – Orval Kent Foods is voluntarily recalling approximately 23,000 pounds of Amish Macaroni Salad that may pose a health risk.

This voluntary action is being taken in response to the results of a test conducted on a single package of Amish Macaroni Salad by the Ohio Department of Agriculture and Consumer Services, Division of Food Safety, for E. coli O157:H7.  

It is important to note that no illnesses associated with consumption of this product have been reported.

The only product included in this recall is Amish Macaroni Salad with the following UPC codes and associated Use By dates:

UPC 7945368281 Orval Kent Amish Macaroni Salad, 5 pound container, Use By 6/12/08
UPC 7347468281 Yoder’s Amish Macaroni Salad, 1 pound container, Use By 6/7/08
UPC 7347401045 Yoder’s Amish Macaroni Salad, 2 pound container, Use by 6/7/08
UPC 7347488729 Yoder’s Amish Macaroni Salad, 5 pound container, Use By 6/7/08
This specific product was shipped to customers who have distribution to retail and food service establishments in the following areas:  Delaware, Illinois, Indiana, Maryland, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

E. coli O157:H7 causes a diarrheal illness often with bloody stools.  Although most healthy adults can recover completely with a week, some people can develop a form of kidney failure that can lead to serious kidney damage and even death.  Young children, the elderly and those with weak immune systems are most susceptible to foodborne illnesses.

No other Yoder’s or Orval Kent deli salads, or other code dates or UPC’s of the Amish Macaroni Salad are included in this recall.

Our highest priority is protecting the health and safety of our customers, consumers and their families.  Today’s precautionary action is a measure to ensure this priority is carried out, and that we maintain the loyalty and trust of our consumers.

Consumers are urged to return all un-opened containers to their place of purchase for a full refund.

Consumers with any questions may contact Orval Kent at 1-800-544-1246.

Fresca Italia, Inc., Recalls Burrata Because of Possible Health Risk

Contact:
Fresca Italia, Inc.
415-468-9800

FOR IMMEDIATE RELEASE -- May 30, 2008 -- Fresca Italia of Brisbane, CA is recalling Burrata because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious 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 fever, headache, stiffness, nausea, abdominal, or diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.

This product was distributed in the San Francisco Bay Area and Southern California in retail stores and restaurants.

This product weighs approximately 8.8oz and is packaged in a white and green plastic wrapper with the manufacturer’s name, “Caseificio Voglie di Latte” and the product name “Burrata” The only batch subject to the recall will be labeled with the expiration date of 24/5/2008.

The recall is the result of survey sampling by the California Dept. of Food & Agriculture which revealed that the product in question contained the bacteria. Fresca Italia has immediately halted further distribution.

If you have any Caseificio Voglie di Latte Burrata with an expiration of 24/5/2008 please return it to the place of purchase for a full refund. Consumers with questions may contact the company at 415-468-9800.

FDA Warns Consumers in New Mexico and Texas Not to Eat Certain Types of Raw Red Tomatoes


The Food and Drug Administration is alerting consumers in New Mexico and Texas that a salmonellosis outbreak appears to be linked to consumption of certain types of raw red tomatoes and products containing raw red tomatoes. The bacteria causing the illnesses are Salmonella serotype Saintpaul, an uncommon type of Salmonella.

The specific type and source of tomatoes are under investigation. However, preliminary data suggest that raw red plum, red Roma, or round red tomatoes are the cause.  At this time, consumers in New Mexico and Texas should limit their tomato consumption to tomatoes that have not been implicated in the outbreak. These include cherry tomatoes, grape tomatoes, tomatoes sold with the vine still attached, and tomatoes grown at home.

Salmonella can cause serious and sometimes fatal infections particularly in young children, frail or elderly people, and those with weakened immune systems. Healthy persons often experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, the organism can get into the bloodstream and produce more severe illnesses.  Consumers in New Mexico and Texas who have recently eaten raw tomatoes or foods containing raw tomatoes and are experiencing any of these symptoms should contact their health care provider. All Salmonella infections should be reported to state or local health authorities.

From April 23 though June 1, 2008, there have been 57 reported cases of salmonellosis caused by Salmonella Saintpaul in New Mexico and Texas, including 17 hospitalizations.  Approximately 30 reports of illness in Arizona, Colorado, Idaho, Illinois, Indiana, Kansas, and Utah are currently being investigated to determine whether they are also linked to tomatoes. There are no reported deaths.

FDA recognizes that the source of the contaminated tomatoes may be limited to a single grower or packer or tomatoes from a specific geographic area.  FDA also recognizes that there are many tomato crops across the country and in foreign countries that are just becoming ready for harvest or will become ready in the coming months.  In order to ensure that consumers can continue to enjoy tomatoes that are safe to eat, FDA is working diligently with the states, the Centers for Disease Control and Prevention, the Indian Health Service, and various food industry trade associations to quickly determine the source and type of the contaminated tomatoes.  As more information becomes available, FDA will update this warning.

Last year FDA began a multi-year Tomato Safety Initiative to reduce the incidence of tomato-related foodborne illness. The Initiative is a collaborative effort between FDA and the state health and agriculture departments in Virginia and Florida, in cooperation with several universities and members of the produce industry.

A key element of the Food Protection Plan -- a scientific and a risk-based approach to strengthen and protect the nation's food supply—is prevention. FDA encourages producers to critically reexamine their operations and apply the scientific principles and regulations established decades ago to provide a safe product for the consumer. 

Information on safe handling of produce can be found at www.cfsan.fda.gov/~dms/prodsafe.html.

Tomato consumer page can be found at http://www.fda.gov/oc/opacom/hottopics/tomatoes.html

Updates from the Centers for Disease Control and Prevention can be found at http://www.cdc.gov/

Tipu's Tiger Chai, Inc Recalls Tipus Tiger Chai Concentrate Because of a Possible Health Risk

Contact:
Bipin Patel
(406) 240 9979

FOR IMMEDIATE RELEASE -- June 17, 2008 -- Tipu's Tiger Chai Inc, of Missoula, Montana is voluntarily recalling its Tipu's Tiger Chai Concentrate 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 after consuming this product should seek immediate medical attention.

Tipu's Tiger Chai Concentrate was distributed, primarily to stores and coffee kiosks in western Montana and one café in Prescott, Arizona using the concentrate for mixed beverages sold on-site. Limited distribution of the bottled product was made directly to consumers in Western Montana.

The product is distributed in plastic half gallon (1.89L) units labeled as "Tipu's Tiger Chai, Chai Concentrate". The lid or neck of bottle states "refrigerate after opening" followed by dates of 09/23/09 through and including 05/22/10.

Please note that NO illnesses have been reported to date.

Through a records audit, the pH level of the product manufactured during this period were found to be higher than required by FDA standards.

Any consumers who may have purchased this product are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-(888)-506-2424.

Matterhorn Group Inc. Announces Voluntary Recall of "Astro Pops" and "Missile Pops" 3.5 oz Cherry Pineapple Frozen Novelty Pops in Arizona, Nevada and California due to Safety Hazard

Contact:
Matterhorn Group Inc.
1-888-264-0898.

FOR IMMEDIATE RELEASE -- June 18, 2008, Boise, ID – Matterhorn Group Inc is recalling certain date coded product of their Rainbow Glacier "Astro Pops" water ice frozen novelty pops, Cherry Pineapple Swirl 3.5 oz size 12 count bag pack, with tag closure "Best by JUN 03-09", "Best by JUN 04-09" and "Best by JUN 05-09" sold through the Wal-Mart stores located in California and Arizona, Sunnyside Farms "Missile Pops" Cherry Pineapple in 3.5 oz. size 12 count bag packages, with tag closure of "Best By JUN 02-09", "Best by JUN 03-09", and "Best by JUN 04-09" sold through the California stores of grocery retailers Save Mart and Raley’s, and Vitafreze Frozen Astronot Pops 3.5 oz size 12 count bag packages, with tag closure of "Best By JUN 02-09" sold in California. The products are being recalled because they may contain pieces of hard plastic. Only the noted product date codes listed are affected.

The small pieces of non-toxic hard plastic were from a part of the processing equipment which broke during the manufacturing process. The majority of the possibly affected product was retrieved from the distribution system before any release to retail stores. However, there were a small number of cases which were shipped to above mentioned locations.

There have been no reports of injury. People who bite into or swallow a fragment could possibly be injured, prompting this precautionary recall. Young children are particularly at risk of a choking hazard. Although the company believes the problem is very isolated, we are taking this measure to ensure the safety of our consumers.

Consumers in AZ and CA who have purchased the above indicated products should return them to their retailer where purchased for a full refund. For questions and inquiries, consumers may contact us at 1-888-264-0898.

Giant Food Alerts Customers to Voluntary Recall of Giant Brand Garlic Bread and Garlic Spread

Contact:
Jamie Miller
(301) 341-8776

FOR IMMEDIATE RELEASE -- June 27, 2008 - Landover, MD -- Giant Food has announced a voluntary recall of Giant brand garlic bread and garlic spread products sold in its Bakeshop as the items contain milk products which are not declared on the labels. Giant removed from its shelves all 16 ounce packages of Giant brand garlic bread and all 16 ounce packages of Giant brand garlic spread products. 

The following products are affected by this recall:

16 oz. Giant Garlic Bread: UPC #21476670000
16 oz. Giant Garlic Spread: UPC #20173310000
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.  No illnesses have been reported.

Customers who have purchased the affected products may return them to Giant for a full refund. Customers looking for additional information may call Giant Customer Service at (888) 469-4426 for more information. Customers can also visit the Giant website at www.giantfood.com.

Haven't said it in awhile, but thanks for keeping us informed Sticks!  It is amazing at the recalls that you never even hear of...scary!

Salmolux Inc. Recalls Wild Alaskan Smoked Salmon Nova Lox Lot # 01418 Because of Possible Health Risk

Contact:
Kira Kuetgens
(253) 874-2026 x 214

FOR IMMEDIATE RELEASE -- Federal Way, WA -- July 9, 2008 --- Salmolux Inc. of Federal Way, WA, is recalling lot # 01418 of its Wild Alaskan Smoked Salmon Nova Lox sold in 3 ounce packages due to 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.

The recalled lot # 01418 of Wild Alaskan Smoked Salmon Nova Lox was distributed in Arizona, California, and Nevada, in Von's retail outlets and to Delaware, Florida, Georgia, Maryland, North Carolina, Pennsylvania, South Carolina, West Virginia, and Virginia in Food Lion retail outlets.

The product comes in a 3 ounce, blue package marked with lot # 01418 on its rear white label bearing the name of the product, its ingredients, and an expiration date.

No illnesses have been reported to date in connection with this problem.

After routine testing by the Florida Department of Agriculture and Consumer Services, Listeria monocytogenes was found in 3 ounce packages of Wild Alaskan Smoked Salmon Nova Lox.

Consumers who have purchased the recalled 3 ounce packages bearing the lot # 01418 of the salmon are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (253) 874-2026 x214.

This recall is being conducted with the knowledge of the Food and Drug Administration.

NOTE: "According to the Texas and North Carolina Departments of Health, the strain of Salmonella found in this company's jalapeño and serrano peppers and in its avocado is not Salmonella Saintpaul, and is not believed to be related to the current Salmonella outbreak.

The recall is a result of sampling not by the U.S. Food and Drug Administration (FDA) but by the Texas Department of State Health Services (Texas Health) and the North Carolina Department of Health and Human Services (North Carolina Health ) which revealed that these products contained the bacteria.

The company has voluntarily initiated a recall of its already distributed products and has stopped future distribution while the FDA, Texas Health, North Carolina Health and the company continue to investigate to determine the source of the problem."


Grande Produce, LTD.CO Recalls Jalapeno Peppers, Serrano Peppers, and Avocados Because of Possible Health Risk

Contact:
Raul Cano
956- 843-8575

FOR IMMEDIATE RELEASE -- July 19, 2008 -- Grande Produce, LTD. CO of Hidalgo, Texas (hereinafter referred to as Grande Produce) is recalling Jalepeno Peppers and Serrano Peppers distributed between May 17th and July 17th, 2008; and Avocados, all sizes, with lot #HUE08160090889 because they have the potential to be contaminated with Salmonella, an organism which 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 (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The Jalapeno Peppers, Serrano Peppers and Avocados were distributed to the following states: TX, DE, NC, GA, OK, IA, MN, IL, FL, IN, MD, NY, MS, AR, KS, and KY.

The avocados being recalled were shipped in boxes labeled "Frutas Finas de Tancitaro HASS Avocados, Produce of Mexico," all sizes, with lot number HUE08160090889. The Jalapeno Peppers and Serrano peppers being recalled were shipped in 35lb. plastic crates with no brand name or label.

No illnesses associated with this recall have been reported to date.

The recall is a result of sampling by the Texas Department of State Health Services and The North Carolina Department of Health and Human Services, which revealed that these products contained the bacteria. Distribution of these products has been suspended while FDA, the Texas Department of State Health Services, The North Carolina Department of Health and Human Services and the company continue their investigation as to the source of the problem.

Consumers who purchased Avocados, Jalapeno Peppers and Serrano Peppers should contact their supplier to determine if their products are involved in the recall. Consumers with questions may contact the company at (956) 843-8575.