Food recall
John Nagle Co. recall: John Nagle Steelhead Fillets
John Nagle Co., of Boston, MA, recalled John Nagle Steelhead Fillets. The FDA's reason: “Product may be contaminated with Listeria monocytogenes.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on November 5, 2020, and the FDA first listed it in its Enforcement Report of November 25, 2020. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class II
It could cause temporary or minor harm
Why
Listeria
Status
Terminated
Closed December 18, 2020
The recall
- Company
- John Nagle Co. (Boston, MA)
- Reason, in FDA's words
- “Product may be contaminated with Listeria monocytogenes.”
- Where it was sold
- MA, NY, PA, OH
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 86722
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-0120-2021 Class II
John Nagle Steelhead Fillets; 1/3 lb; Iceland; N44515; Habrun ehf; Packaging date: 29 10 2020
Codes: Packaging Date: 29 10 2020 N44515 Distributed on 11/3 and 11/4/2020
Quantity: 5x10kg
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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 25, 2020.
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.