FDA Drug Recalls

Recalls / Class II

Class IID-0421-2025

Product

Artridon Glucosamine (menthol 2% and Methyl Salicylate 15% - Topical Analgesic), for arthritis joint pain relief, 5 oz (142g) Tube, Dist by/por: Pharmadel LLC, New Castle, DE, 19720, Made in India, NDC 55758-030-05, UPC 8 10096 77151 3.

Brand name
Artridon
Generic name
Menthol, Methyl Salicylate
Active ingredients
Menthol, Unspecified Form, Methyl Salicylate
Route
Topical
NDC
55758-030
FDA application
M017
Affected lot / code info
Lot SP25A, Exp Date: 09/30/2026

Why it was recalled

CGMP Deviations

Recalling firm

Firm
KENIL HEALTHCARE PRIVATE LIMITED
Manufacturer
Pharmadel LLC
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
9,984 Tubes
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-0421-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.