Artridon Glucosamine recalled over manufacturing violations
- Recall date
- April 24, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- KENIL HEALTHCARE PRIVATE LIMITED recalls Artridon Glucosamine (menthol 2% and Methyl Salicylate 15% - Topical Analgesic), for arthritis joint pain relief, 5 oz…
- Recall number
- D-0421-2025
- FDA classification
- Class II
- Brand / firm
- KENIL HEALTHCARE PRIVATE LIMITED
- Sold / distributed
- DE and NC
Why it was recalled
CGMP Deviations
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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.
Get recall alerts
Free email alert whenever KENIL HEALTHCARE PRIVATE LIMITED has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: KENIL HEALTHCARE PRIVATE LIMITED