F-1222-2024 Class III Terminated
FDA food recall F-1222-2024 was initiated by HTO Nevada Inc DBA Kirkman on Mar 12, 2024 and is designated Class III. Reason for recall: 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… The recall status is terminated (terminated Jun 25, 2024). Affected quantity: 366 bottles.
Recall Details
- Product Type
- Food
- Report Date
- May 15, 2024
- Initiation Date
- Mar 12, 2024
- Termination Date
- Jun 25, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 366 bottles
Product Description
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,
Reason for Recall
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).
Distribution Pattern
Distributed in CA, FL, OH, TX, WA and WI and in the following countries China, Netherlands, Pakistan, Peru, Switzerland, and United Kingdom.
Code Information
Lot#: 477-0016, Exp: 08/2025
Source
- Dataset
- openFDA food recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for F-1222-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 23, 2026