Class III Recall — Unlikely to Cause Adverse Health Consequences

HTO Nevada Inc DBA Kirkman Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule dietary supplement, Fola Recall 2024

Official title: 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,

FoodBy Recall Watch Editorial TeamMarch 12, 2024Updated April 27, 2026

Verified source

U.S. Food and Drug Administration

This summary mirrors the official FDA notice issued March 12, 2024. Last synced from FDA: Apr 27, 2026.

Read official FDA notice

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,

FDAClass III — Low Riskfood

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,

Affected Lot Numbers

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

Lot Number
Lot#: 477-0016
Exp: 08/2025

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).

Where was it sold

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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What to do

  1. Do not consume or use this product
  2. Check the lot numbers or UPC codes listed above
  3. Return the product to the store where you purchased it for a full refund
  4. Contact your healthcare provider if you have experienced any symptoms
View official FDA notice

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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.

Why was HTO Nevada Inc DBA Kirkman recalled in 2024?

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).