Food recall
Bix Produce Company LLC recall: FreshPoint Bix Produce Company, Cantaloupe
Bix Produce Company LLC, of Little Canada, MN, recalled FreshPoint Bix Produce Company, Cantaloupe. The FDA's reason: “Cantaloupe may be contaminated with Salmonella.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on September 29, 2023, and the FDA first listed it in its Enforcement Report of November 8, 2023. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class I
It could cause serious harm or death
Why
Salmonella
Status
Terminated
Closed January 11, 2024
The recall
- Company
- Bix Produce Company LLC (Little Canada, MN)
- Reason, in FDA's words
- “Cantaloupe may be contaminated with Salmonella.”
- Where it was sold
- IA, MN, ND, WI
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 93162
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-0304-2024 Class I
FreshPoint Bix Produce Company, Cantaloupe. Item # 03143. 3 melons per bag.
Codes: Bix Lot Numbers: P2742702-00 and P2741287
Quantity: 61 - 3 packs
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of November 8, 2023.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.