Recall Atlas
Food & drinkClass III

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

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.

Read the official notice →
Date
2023-11-29
Country
United States
Brand
ActiPharma, Inc.
Product
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Classification
Class III
Units
Domestic distribution, in Puerto Rico.
Category
Food & drink
Source
FDA · Food

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, pack size, batch or lot code and best-before date against the official notice.
  2. If it matches, do not eat or drink it. Return it to the shop for a refund or throw it away as the notice says.
  3. If you have eaten it and feel unwell, contact a doctor or your local health service and mention the recall.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

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