Home / ActiPharma, Inc. / F-0463-2024
Class III
ActiPharma, Inc.
Recall #F-0463-2024 · Initiated 2023-09-28
Product
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.
Quantity affected
607 bottles of 100 tablets each
Distribution
Domestic distribution, in Puerto Rico.
Lot / code info
Lot 13309, Exp: 01/26
Voluntary / mandated
Voluntary: Firm initiated
Initial notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Terminated
2024-01-16
Recalling firm
ActiPharma, Inc.
Carretera No. 1, Km. 21.1
Guaynabo, PR 00971
United States
Recall classification
Unlikely to cause any adverse health consequences.