Turtle Pie Recalled

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Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



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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FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

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