FDAFDA · Food and drugs·Recall number F-0463-2024
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Published November 29, 2023 · Recall initiated: September 28, 2023
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- ActiPharma, Inc.
- Distributor
- Domestic distribution, in Puerto Rico.
- Lot
- Lot 13309, Exp: 01/26
- Risk classification
- Class III
- Area (FDA)
- food
- Country
- United States
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