Food recall
FLP LLC recall: Dr
FLP LLC, of Tempe, AZ, recalled Dr. The FDA's reason: “Colostrum is declared but label does not declare milk.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on March 29, 2023, and the FDA first listed it in its Enforcement Report of May 17, 2023. The recall is still going on.
How serious
Class II
It could cause temporary or minor harm
Why
Allergen not on the label
Status
Ongoing
The recall
- Company
- FLP LLC (Tempe, AZ)
- Reason, in FDA's words
- “Colostrum is declared but label does not declare milk.”
- Where it was sold
- Distributed in CA, FL, NJ, and NY.
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 92087
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-0822-2023 Class II
Dr. Rico Perez Super Kids Colostrum, 60 count chewable tablets dietary supplement, Supplement Facts: 200 mg Colostrum per 1 tablet. HDPE bottle. UPC 8 79840 00044 6. Mfg For: Rico Perez Prod., In2295 Coral Way, Miami, FL 33145.
Codes: Lot Code 1117002, Expiration Date 04/30/2023. Lot Code 0122003, Expiration Date 07/31/2024. Lot Code 0223539, Expiration Date 11/30/2025.
Quantity: Lot 1117002 = 5,760 bottles; Lot 0122003 = 1,800 bottles; Lot 0223539 = 180 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 May 17, 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.