Food recall
Bountiful Trading Inc recall: Kroger brand, Vitamin D3 125 mcg softgels
Bountiful Trading Inc, of New York, NY, recalled Kroger brand, Vitamin D3 125 mcg softgels. The FDA's reason: “Vitamin D dietary supplement may contain Coq10.” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on July 9, 2021, and the FDA first listed it in its Enforcement Report of July 28, 2021. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class III
It is unlikely to cause harm
Why
See FDA's words below
Status
Terminated
Closed May 19, 2022
The recall
- Company
- Bountiful Trading Inc (New York, NY)
- Reason, in FDA's words
- “Vitamin D dietary supplement may contain Coq10”
- Where it was sold
- IN, TN, WI, CO, AZ
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 88263
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-0789-2021 Class III
Kroger brand, Vitamin D3 125 mcg softgels, 100 count, Green HDPE packaging
Codes: Prod # 19937, Lot # 508981-02, Exp 02/24 041260351211
Quantity: 12,360 bottles
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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 July 28, 2021.
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.