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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

ActiPharma, Inc. 2023-11-29 Food moderate FDA
Food · FDA · Recall #FDA-F-0463-2024

ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309,… Recall

Issued November 29, 2023 · ActiPharma, Inc.

In November 2023, ActiPharma, Inc. recalled the ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309,…, a moderate food recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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 you should do

  1. 1 Stop using ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309,… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact ActiPharma, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
ActiPharma, Inc.
Category
Food
Recall date
November 29, 2023
Units affected
Not reported
Sold at
Domestic distribution, in Puerto Rico.
Recall number
FDA-F-0463-2024
Made in
United States
Issuing agency
FDA

In context

  • ActiPharma, Inc. has 1 recall in our database.
  • We're tracking 3,082 Food recalls in our database.
  • This is the 886th Food recall we've logged in 2023.
Read the official FDA notice

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