---
title: "ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (... — FDA record F-0463-2024 | Is It on Recall"
description: "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."
url: https://isitonrecall.com/recall/fda-food-f-0463-2024-actiron-dietary-supplement-actipharma-100-tablets-24-bottles-per-case-lot-13309-exp-01-26-upc-363102/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104. — FDA record F-0463-2024

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 28, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
- **Reason**: 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.
- **Classification**: Class III
- **Recalling firm**: ActiPharma, Inc.
- **Quantity**: 607 bottles of 100 tablets each
- **Agency-reported status**: Terminated
- **Source record identifier**: F-0463-2024

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0463-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot 13309, Exp: 01/26 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic distribution, in Puerto Rico.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Nov 29, 2023
- **Recall initiation date**: Sep 28, 2023
- **Center classification date**: Nov 17, 2023
- **Termination date**: Jan 16, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0463-2024%22)

## Related records

[Supplements records](https://isitonrecall.com/product/supplements/) [Supplements records](https://isitonrecall.com/category/supplements/) [ActiPharma, Inc. records](https://isitonrecall.com/brand/actipharma-inc/)