Food Enforcement F-1222-2024

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).

Status

Terminated

Classification

Class III

Report Date

May 15, 2024

Recall Initiation

March 12, 2024

Product Information

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,
Product quantity
366 bottles
Product type
Food
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).
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Distribution pattern
Distributed in CA, FL, OH, TX, WA and WI and in the following countries China, Netherlands, Pakistan, Peru, Switzerland, and United Kingdom.

Location & Firm

Recalling firm
HTO Nevada Inc DBA Kirkman
Address
6400 Rosewood St, N/A

United States
Voluntary / Mandated
Voluntary: Firm initiated

Codes & Dates

Recall number
F-1222-2024
Event ID
94230
Recall initiation date
March 12, 2024
Center classification date
May 8, 2024
Code info
Lot#: 477-0016, Exp: 08/2025
More code info