HTO Nevada Inc DBA Kirkman: Food Recall
Recall #F-1222-2024 · 03/12/2024
Class III: Low Risk
Recall Details
- Recall Number
- F-1222-2024
- Classification
- Class III
- Product Type
- Food
- Recalling Firm
- HTO Nevada Inc DBA Kirkman
- Status
- Terminated
- Date Initiated
- 03/12/2024
- Location
- Lake Oswego, OR, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 366 bottles
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).
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,
Distribution Pattern
Distributed in CA, FL, OH, TX, WA and WI and in the following countries China, Netherlands, Pakistan, Peru, Switzerland, and United Kingdom.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.