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ActiPharma, Inc.

1 recall record in Supplements.

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2023

1 record

Class IIITerminatedRecall F-0463-2024

Product description

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.

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Event ID
93210
Code info
Lot 13309, Exp: 01/26
Product quantity
607 bottles of 100 tablets each
Distribution pattern
Domestic distribution, in Puerto Rico.
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product type
Food
Recalling firm location
Carretera No. 1, Km. 21.1, Sector La Muda, Guaynabo, PR, United States
Recall initiation date
09/28/2023
Center classification date
11/17/2023
Termination date
01/16/2024