Recall record at a glance
| Official record | F-0180-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Bonduelle USA Inc. |
| Report date | Nov 18, 2015 |
| Recall initiation date | Aug 28, 2015 |
| Quantity | 9,335 cases |
| Location | Brockport, NY, United States |
Official product description
Frozen Corn distributed under the following labels and sizes: (a) WYLWOOD Super Sweet Whole Kernel Corn, NET WT. 16 OZ (1 LB), UPC 051933002401, DISTR. BY: SAVE-A-LOT FOOD STORES LTD. EARTH CITY, MO 63045; (b) MARKET BASKET Cut Corn, NET WT. 16 OZ. (1 LB.), UPC 049705693414, Packed Exclusively for: DEMOULAS SUPERMARKETS, INC. Tewksbury, MA 01876; (c) Bountiful Harvest WHOLE KERNEL CUT CORN, NET WT. 40 OZ. (2.5 LBS.), UPC 822486120597, Marketed by: Independent Marketing Alliance Houston, TX 77079; (d) WEST CREEK FROZEN VEGETABLES Cut Corn, NET WT. 2.5 LBS., UPC 00806795285239. --- The product is packed in poly bags.
Why the product was recalled
One code of Wylwood brand Frozen Whole Kernel Corn was found to be contaminated with Listeria monocytogenes based on sampling and analysis by the State of Tennessee. The firm decided to recall other labels and codes produced the same day as the suspect lot as a precaution.
Distribution information
New York, New Jersey, Pennsylvania, Vermont, Massachusetts, Indiana, Ohio, Kentucky, Maryland, Virginia, North Carolina, Florida, Mississippi and Louisiana.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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