US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 24, 2025 (17 months ago)

KOFAL Original, Penetrating Pain Relieving Ointment (methyl salicylate 12% - Topical…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations

What was recalled

KOFAL Original, Penetrating Pain Relieving Ointment (methyl salicylate 12% - Topical Analgesic), 4 oz (113 g) Jar, Distributed by: Pharmadel LLC, Georgetown, DE 199747, NDC 55758-106-04, UPC 8 9971100128 0.

Recalling firm
Kenil Healthcare Private Limited
NDC code
55758-106-04
Origin
N/A, India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0425-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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