Skip to main content

← Back to recall

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

Answers to common safety, symptoms, and disposal questions for this specific recall.

Key recall facts

  • Brand: HTO Nevada Inc DBA Kirkman
  • 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).
  • Published: 3/12/2024

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).