LOW RISK
Terminated
F-0463-2024
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Recalled by ActiPharma, Inc.
Classification
Class III — Products that are unlikely to cause any adverse health reaction, but that violate FDA labeling or manufacturing laws.
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.
Product Details
Product Quantity
607 bottles of 100 tablets each
Product Type
Food
Code Info
Lot 13309, Exp: 01/26
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Domestic distribution, in Puerto Rico.
Company Location
Guaynabo, PR, 00971
Timeline
Report Date
11/29/2023
Recall Initiated
09/28/2023
Classification Date
11/17/2023
Termination Date
01/16/2024
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 29, 2026
Related Recalls
Get Real-Time Recall Alerts on Your Phone
Scan any grocery receipt and instantly know if your food has been recalled. Free download — protect your family in 3 seconds.
