ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/...

FDA Recall #F-0463-2024 — Class III — September 28, 2023

Recall #F-0463-2024 Date: September 28, 2023 Classification: Class III Status: Terminated

Product Description

ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.

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.

Recalling Firm

ActiPharma, Inc. — Guaynabo, PR

Classification

Class III — A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.

Product Type

Food

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated