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HTO Nevada Inc DBA Kirkman

HTO Nevada Inc DBA Kirkman Recalls

All product recalls associated with HTO Nevada Inc DBA Kirkman.

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Mar 2024

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

5-MTHF Methylfolate Capsules (Kirkman) – Labeling Error (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).

Class IIILow

FDAMar 12, 2024CA, FL, IN +4 more• HTO Nevada Inc DBA Kirkman

Maximum Zone2 Topical Analgesic (HTO Nevada) – Raw Material Issue (2023)

cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.

Class IIModerate

FDAFeb 9, 2023Nationwide• HTO Nevada, Inc.

Blue Gel Anesthetic (HTO Nevada) – Raw Material Issue (2023)

cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.

Class IIModerate

FDAFeb 9, 2023Nationwide• HTO Nevada, Inc.