Class IIILow risk
ACTIRON: Dietary supplement
FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.
The recalled product
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Codes on the package: Lot 13309, Exp: 01/26
This recall is no longer in progress, but product already in your home is still recalled. If you have this product, don’t eat it or feed it. Throw it away, or return it where you bought it.
- Status
- Closed by the FDA (Terminated)
- Type
- Food
- Recalled by
- ActiPharma, Inc.
- Posted by the FDA
- Started by the firm
- Classified
- Sold in
- Domestic distribution, in Puerto Rico.
From the FDA
This recall is in the FDA’s Enforcement Report under recall number F-0463-2024. The headline above is a summary; the product descriptions are the FDA’s own words.