FDA Drug Recalls

Recalls / Class II

Class IID-0425-2025

Product

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.

Affected lot / code info
Lost SP21A, Exp Date: 03/31/2026

Why it was recalled

CGMP Deviations

Recalling firm

Firm
KENIL HEALTHCARE PRIVATE LIMITED
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
Plot 319, Village Acharasan, Ankhol-Vamaj Road, Ta. Kadi, District Mehsana, N/A N/A, India

Distribution

Quantity
16,248 Jars
Distribution pattern
DE and NC

Timeline

Recall initiated
2025-04-24
FDA classified
2025-05-19
Posted by FDA
2025-05-28
Terminated
2026-02-19
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0425-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.