Food Recall Check
Class III · Low risk Terminated Initiated Sep 28, 2023 (3 years ago)

ACTIRON Dietary Supplement recall

Recalled by ActiPharma, Inc. · Guaynabo, PR, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

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.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

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

Quantity: 607 bottles of 100 tablets each

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 13309, Exp: 01/26

Where it was sold

Puerto Rico

FDA's distribution note: Domestic distribution, in Puerto Rico.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
ActiPharma, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 28, 2023
In FDA report of
Nov 29, 2023
Terminated
Jan 16, 2024
FDA recall number
F-0463-2024 · event 93210
Official record
FDA enforcement report search

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