WHY THIS PRODUCT IS LISTED
Other / see reason
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 & recall reason
The recall record describes “ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.”; the source reports: “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.”
Based on the official recall record; packaging and sales claims have not been verified. Verify with the official source ↗
Identify the product
- Product description
- ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
- Brand
- Not supplied by this source
- Lot, batch, UPC & other codes
- Lot 13309, Exp: 01/26
- Quantity
- 607 bottles of 100 tablets each
Where it came from & where it went
- Recalling firm
- ActiPharma, Inc.
- Recalling firm address
- Carretera No. 1, Km. 21.1; Sector La Muda; Guaynabo; PR; 00971; United States
- Product production / origin location
- Not supplied by this source
- Distribution — source wording
- Domestic distribution, in Puerto Rico.
States identified in the source
Puerto Rico
State matching is derived from the source’s distribution wording, which may be incomplete. The recalling company’s address is not used as the distribution location.
A recalling firm’s address is not necessarily where the food was grown or manufactured. Distribution can change; check the official notice.