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RECALL RECORD — CLASS IIIRecall closedF-0463-2024/FDA enforcement
Actipharma, INC.·Dietary Supplements·Sep 28, 2023

Actiron Dietary Supplement, Actipharma, 100 Tablets (24 Bottles Per Case) ) (

What you need to know

Class III

  • What happened

    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.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDAINMore supplements

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Product identification

Source: FDA FOOD

Brand nameActipharma, INC.
Recalling firmActipharma, INC.Guaynabo, PR, United States
UPC / barcodes
3 63102 21710 4
Lot / date codes
  • Lot 13309, Exp: 01/26
Distribution area
IN

Domestic distribution, in Puerto Rico.

United States, Puerto Rico

Quantity affected607 bottles of 100 tablets each
Recall initiationFDA report date: November 29, 2023
FDA recall numberF-0463-2024

Beyond the headline

The recall, in context

Actipharma, INC. initiated this supplements recall on September 28, 2023. The FDA enforcement report states: 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. The FDA report lists distribution as: Domestic distribution, in Puerto Rico.

The FDA enforcement report describes the reason as: 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.

Actiron Dietary Supplement, Actipharma, 100 Tablets (24 Bottles Per Case) ) ( was made or distributed by Actipharma, INC. in Guaynabo, PR, United States. This page reflects FDA report F-0463-2024, dated November 29, 2023.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Actiron Dietary Supplement, Actipharma, 100 Tablets (24 Bottles Per Case) ) ( recall?

Actipharma, INC. recalled Actiron Dietary Supplement, Actipharma, 100 Tablets (24 Bottles Per Case) ) ( in an FDA Class III enforcement action reported as F-0463-2024. 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.

What are the symptoms of Product safety recall exposure?

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Who is most at risk from Product safety recall?

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

How do I get a refund from Actipharma, INC.?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0463-2024 and keep the packaging, lot code and proof of purchase if you have them.

Is the Actipharma, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0463-2024. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.