More Than 9,000 Cases Of Frozen Corn Recalled
PHILADELPHIA (CBS) -- Check your freezer: Bonduelle USA is recalling more than 9,000 cases of frozen corn.
According to a statement on the FDA website, Bonduelle USA Inc. of Brockport, NY is recalling 9,335 cases of frozen corn 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, according to the statement.
The frozen cut corn was distributed to stores in the following states: New York, New Jersey, Pennsylvania, Vermont, Massachusetts, Indiana, Ohio, Kentucky, Maryland, Virginia, North Carolina, Florida, Mississippi and Louisiana, according to the statement.
The statement says the affected frozen cut corn was distributed in poly bags under the following labels and codes:
- WYLWOOD Super Sweet Whole Kernel Corn, NET WT. 16 OZ (1 LB), UPC 051933002401, Codes: Best By June 2017 K51564 and K51574;
- MARKET BASKET Cut Corn, NET WT. 16 OZ. (1 LB.), UPC 049705693414, Code: Best By June 2017 K51574;
- Bountiful Harvest WHOLE KERNEL CUT CORN, NET WT. 40 OZ. (2.5 LBS.), UPC 822486120597, Code: Best By June 2017 K51574;
- WEST CREEK FROZEN VEGETABLES Cut Corn, NET WT. 2.5 LBS., UPC 00806795285239 Code: Best By June 2017 K51574.
The company has not received any complaints in relation to this product and is not aware of any illnesses associated with the product to date, according to the statement.
The statement says the recall was the result of product being tested at retail by the State of Tennessee which had tested positive for Listeria monocytogenes. The company has ceased distribution of the product, and the company and US Food and Drug Administration (FDA) continue their investigation as to what caused the problem, according to the statement, which also says the company is fully cooperating with the FDA.
Consumers who purchased the product are urged not to consume this product and throw it away. Consumers requiring refund or with questions may contact the company at 1-877-990-2662, Monday - Friday, 9 am - 4 pm EST.
For more information, visit: http://www.fda.gov/Safety/Recalls/ucm460634.htm
