Artridon Glucosamine recall: CGMP Deviations
Artridon Glucosamine (menthol 2% and Methyl Salicylate 15% - Topical Analgesic), for arthritis joint pain relief, 5 oz (142g) Tube, Dist by/por…
Why was Artridon Glucosamine recalled?
CGMP Deviations
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot SP25A, Exp Date: 09/30/2026
- Product
- Artridon Glucosamine (menthol 2% and Methyl Salicylate 15% - Topical Analgesic), for arthritis joint pain relief, 5 oz (142g) Tube, Dist by/por…
- Recalling firm
- KENIL HEALTHCARE PRIVATE LIMITED
- Quantity
- 9,984 Tubes
- Distribution
- DE and NC
- Recall date
- May 28, 2025
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)