FDA recall F-0463-2024

ActiPharma, Inc. · Class III · food

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.

Distribution

Domestic distribution, in Puerto Rico.

Key facts

Status
Terminated
Initiation date
2023-09-28
Report date
2023-11-29
Termination date
2024-01-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
Guaynabo, PR, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-0463-2024