Kenil Healthcare recalls Artridon Glucosamine topical analgesic for arthritis pain due to manufacturing quality control deviations. This product may not meet safety standards.
CGMP Deviations
Kenil Healthcare is recalling Artridon Glucosamine topical pain relief for arthritis. The product was made with manufacturing quality control issues that could affect safety.
The product was made with manufacturing quality control deviations (CGMP deviations). This means the product may not meet safety standards, but the specific risk is not clearly described in the recall.
People who own or use the Artridon Glucosamine 5 oz tube for arthritis pain relief are affected. Those with arthritis who use this product are most at risk.
Check for the Artridon Glucosamine 5 oz tube labeled with NDC 55758-030-05. The product was made in India with lot number SP25A and expires September 30, 2026.
Look for the NDC code 55758-030-05 on the tube label.
The recall states there were manufacturing quality control deviations (CGMP deviations), but does not specify if the product is safe to use.
The recall does not provide a remedy, so no specific action is required beyond checking if you have the product.
The product was made in India with lot number SP25A and expires September 30, 2026.
We’ve drafted a message you can send Kenil Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0421-2025 — Kenil Healthcare Kenil Healthcare Hello, I own a Kenil Healthcare that is covered by recall D-0421-2025 from Kenil Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
