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RECALL RECORD — CLASS IIIRecall closedF-1222-2024/FDA enforcement
Hto Nevada INC Dba Kirkman·Dietary Supplements·Mar 12, 2024

Kirkman Brand 5-mthf Methyltetrahydrofolate 1mg Capsule Dietary Supplement, Folate 1667mcg Dfe, …

What you need to know

Class III

  • What happened

    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…

  • 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 FDAIN, CA, FL, OH +3 moreMore supplements

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Product identification

Source: FDA FOOD

Brand nameHto Nevada INC Dba Kirkman
Recalling firmHto Nevada INC Dba KirkmanLake Oswego, OR, United States
UPC / barcodes
8 12325 02354 7
Lot / date codes
  • Lot#: 477-0016, Exp: 08/2025
Distribution area
INCAFLOHTXWAWI

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

United States, United Kingdom, China

Quantity affected366 bottles
Recall initiationFDA report date: May 15, 2024
FDA recall numberF-1222-2024

Beyond the headline

The recall, in context

Hto Nevada INC Dba Kirkman initiated this supplements recall on March 12, 2024. The FDA enforcement report states: 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). The FDA report lists distribution as: Distributed in CA, FL, OH, TX, WA and WI and in the following countries China, Netherlands, Pakistan, Peru, Switzerland, and United Kingdom.

The FDA enforcement report describes the reason as: 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).

Kirkman Brand 5-mthf Methyltetrahydrofolate 1mg Capsule Dietary Supplement, Folate 1667mcg Dfe, … was made or distributed by Hto Nevada INC Dba Kirkman in Lake Oswego, OR, United States. This page reflects FDA report F-1222-2024, dated May 15, 2024.

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 Kirkman Brand 5-mthf Methyltetrahydrofolate 1mg Capsule Dietary Supplement, Folate 1667mcg Dfe, … recall?

Hto Nevada INC Dba Kirkman recalled Kirkman Brand 5-mthf Methyltetrahydrofolate 1mg Capsule Dietary Supplement, Folate 1667mcg Dfe, … in an FDA Class III enforcement action reported as F-1222-2024. 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…

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.

Is the Hto Nevada INC Dba Kirkman 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-1222-2024. 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.