Recall record at a glance
| Official record | F-2225-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | The Pictsweet Company |
| Report date | Sep 21, 2016 |
| Recall initiation date | May 6, 2016 |
| Quantity | 871,952 Cases Total |
| Location | Bells, TN, United States |
Official product description
Frozen green peas labeled as: 1. Kroger(R) Green Peas, NET WT 32 OZ (2 LB) 907g, UPC 1111081918 BEST IF USED BY: Jan 2016 through Mar 2016; with Mfg Code ### # K # # 2. p$$t(TM) Green Peas, NET WT 16 OZ (1 LB) 453g, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OH 45202, UPC 1111082603 BEST IF USED BY: Feb 2016 through Mar 2016; with Mfg Code ### # K # # 3. Kroger(R) Green Peas, NET WT 12 OZ. (340g), DISTRIBUTED BY THE KROGER CO., CINCINNATI, OH 45202, UPC 1111089736 BEST IF USED BY: Jan 2016 through Apr 2016; with Mfg Code ### # K # # 4. Pictsweet(R) Green Peas Family Size, NET WT. 28 OZ., 1 LB. 12 OZ. (794g), UPC 7056090056 BEST IF USED BY: Jul 20 2016, Aug 10 2016, Aug 20 2016, Sep 16 2016, Sep 21 2016; with Mfg Code ### # K # # 5. Pictsweet(R) Green Peas Family Size, NET WT. 24 OZ., 1 LB. 8 OZ. (680g), UPC 7056090093 BEST IF USED BY: Aug 20 2016, Sep 10 2016; with Mfg Code ### # K # #
Why the product was recalled
Possible Listeria Monocytogenes contamination in bulk vegetables supplied by CRF Frozen Foods, LLC used in manufacturing several Pictsweet products.
Distribution information
Nationwide
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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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