ActiPharma, Inc. recalls ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.

Recall date

September 28, 2023

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

F-0463-2024

FDA classification

Class III

Brand / firm

ActiPharma, Inc.

Sold / distributed

Domestic distribution, in Puerto Rico.

Why it was 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.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.