Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
ACTIRON Dietary Supplement Recalled by ActiPharma, Inc. Due to FDA sample analysis of ACTIRON Dietary Supplement, 100...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact ActiPharma, Inc. directly.
Affected Products
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Quantity: 607 bottles of 100 tablets each
Why Was This Recalled?
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.
Where Was This Sold?
Domestic distribution, in Puerto Rico.
About ActiPharma, Inc.
ActiPharma, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Food). Last updated March 26, 2026. View original report