ActiPharma, Inc.: Food Recall
Recall #F-0463-2024 · 09/28/2023
Class III: Low Risk
Recall Details
- Recall Number
- F-0463-2024
- Classification
- Class III
- Product Type
- Food
- Recalling Firm
- ActiPharma, Inc.
- Status
- Terminated
- Date Initiated
- 09/28/2023
- Location
- Guaynabo, PR, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 607 bottles of 100 tablets each
Reason for Recall
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.
Product Description
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Distribution Pattern
Domestic distribution, in Puerto Rico.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.