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HTO Nevada Inc DBA Kirkman Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg Recall 2024

HTO Nevada Inc DBA KirkmanIssued March 12, 2024Updated Reviewed by the Recall Watch editorial team

HTO Nevada Inc DBA Kirkman Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule dietary supplement, Folate 1667mcg DFE, 5000mcg Folic Acid, 120 capsules per package, UPC 8 12325 02354 7. Manufactured exclusively by: Kirkman, — recalled per FDA on 3/12/2024. Reason: Labeling error. The 5-MTHF 1mg label incorrectly declares 5000mcg Folic Acid instead 1000mcg Folic Acid per serving in the Supplement Facts, but correctly declares Folate 1667mcg DFE. The front label correctly declares product as 5-MTHF Methyltetrahydrofolate 1mg (or 1000mcg)..

Agency
FDA
Issued
Mar 12, 2024
Brand
HTO Nevada Inc DBA Kirkman
Distribution
6 states
Lots affected
2
What to do right now

Steps to take for this recall

  1. Stop using it

    Take it out of rotation. Don't consume, wear, or operate.

  2. Verify the match

    Compare lot numbers, UPCs, and dates against your product.

  3. Return or dispose

    Follow the manufacturer's instructions to refund or safely dispose.

  4. Clean prep surfaces

    Wash any utensils, cutting boards, or containers that touched the product with hot soapy water.

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Verified summary of the official U.S. Food and Drug Administration notice · Issued March 12, 2024 · Last synced Apr 27, 2026

What's recalled

Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule dietary supplement, Folate 1667mcg DFE, 5000mcg Folic Acid, 120 capsules per package, UPC 8 12325 02354 7. Manufactured exclusively by: Kirkman, Lake Oswego, OR 9703,

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Why it was recalled

Labeling error. The 5-MTHF 1mg label incorrectly declares 5000mcg Folic Acid instead 1000mcg Folic Acid per serving in the Supplement Facts, but correctly declares Folate 1667mcg DFE. The front label correctly declares product as 5-MTHF Methyltetrahydrofolate 1mg (or 1000mcg).

Affected products & lot numbers
2 lots called out

Affected Lot Numbers

Check your product label — do not use if your lot number appears below.

Lot Number
Lot#: 477-0016
Exp: 08/2025
Where was it sold
6 states

Distributed in CA, FL, OH, TX, WA and WI and in the following countries China, Netherlands, Pakistan, Peru, Switzerland, and United Kingdom.

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Official noticefda.gov
More recalls like this
4 related — by brand, contaminant, and category

Frequently asked questions

Is the HTO Nevada Inc DBA Kirkman recall still active?

Yes, this recall is currently active as of March 12, 2024. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: Lot#: 477-0016, Exp: 08/2025. Check the label on your product.

What should I do if I have the recalled HTO Nevada Inc DBA Kirkman?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.