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Supplement Recall Tracker

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F-1222-2024

HTO Nevada Inc DBA Kirkman

Data retrieved 2026-10-27T22:06:49.008Z

Site-assigned category (for this product recall): Allergen & mislabeling

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Official openFDA record · FDA recalls and safety alerts

Fields as reported by FDA

Dates are formatted YYYY-MM-DD. “Not reported” means the field was absent or empty.

recall_number
F-1222-2024
event_id
94230
recalling_firm
HTO Nevada Inc DBA Kirkman
city
Lake Oswego
state
OR
country
United States
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).
classification
Class III
FDA-reported status (not current status)
Terminated
FDA does not update this status after recall classification. It may not reflect whether the recall is currently ongoing, completed, or terminated.
voluntary_mandated
Voluntary: Firm initiated
distribution_pattern
Distributed in CA, FL, OH, TX, WA and WI and in the following countries China, Netherlands, Pakistan, Peru, Switzerland, and United Kingdom.
product_quantity
366 bottles
code_info
Lot#: 477-0016, Exp: 08/2025
recall_initiation_date
2024-03-12
report_date
2024-05-15
termination_date
2024-06-25