Kirkman recalls 120-count 5-MTHF Methyltetrahydrofolate capsules due to labeling error showing 5000mcg Folic Acid instead of 1000mcg per serving. This does not pose a safety risk but may cause confusion about actual folate content.
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 is recalling 120-count 5-MTHF Methyltetrahydrofolate capsules because the label incorrectly lists 5000mcg Folic Acid per serving instead of 1000mcg. This labeling error does not create a safety hazard but could lead to confusion about the actual folate content in the supplement.
The product label incorrectly states 5000mcg Folic Acid per serving when it should be 1000mcg. This labeling error does not cause physical harm but could lead to confusion about the actual folate content in the supplement.
People who purchased Kirkman's 5-MTHF Methyltetrahydrofolate 1mg capsules (120-count) with UPC 8 12325 02354 7 are affected. Those taking folic acid supplements for medical reasons may be most concerned about the labeling discrepancy.
Check for Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsules with 120 count, UPC 8 12325 02354 7, manufactured by Kirkman in Lake Oswego, OR. The product label shows Folate 1667mcg DFE but incorrectly lists 5000mcg Folic Acid instead of 1000mcg.
Verify the label shows Folate 1667mcg DFE but correctly lists 1000mcg Folic Acid per serving (not 5000mcg).
No, this labeling error does not pose a safety risk but may cause confusion about the actual folate content.
Check for Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsules with UPC 8 12325 02354 7, manufactured in Lake Oswego, OR.
No, the labeling error does not create a safety hazard, so you can continue using it but should check the label for accurate information.
We’ve drafted a message you can send Kirkman to request your refund or repair — edit it as you like.
Subject: Recall F-1222-2024 — Kirkman Kirkman Hello, I own a Kirkman that is covered by recall F-1222-2024 from Kirkman. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
