MexHealth recalls 30-count glucosamine curc:uma ortiga tablets containing undeclared diclofenac and methocarbamol. FDA lab tests found these ingredients without proper approval. Stop using immediately.
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac and methocarbamol,
MexHealth is recalling glucosamine curcuma ortiga tablets that contain undeclared diclofenac and methocarbamol. These ingredients were found in the product by FDA lab tests without proper approval, posing a risk of serious health issues.
FDA lab tests found the product contains diclofenac and methocarbamol without proper FDA approval. These ingredients can cause serious health issues if taken without proper medical supervision.
People who own or use the 30-count glucosamine curcuma ortiga tablets from MexHealth. Those with health conditions requiring careful medication use are at higher risk.
Check for the 30-count bottle labeled 'OSSOS-SANS Reforzado con: Glucosamina Curcuma Ortiga'. The lot number is H29585 with no expiration date.
Immediately stop using the recalled tablets as they contain undeclared diclofenac and methocarbamol.
FDA lab tests found the product contains undeclared diclofenac and methocarbamol without proper approval.
Check for the 30-count bottle labeled 'OSSOS-SANS Reforzado con: Glucosamina Curcuma Ortiga' with lot number H29585 and no expiration date.
Immediately stop using the product and contact MexHealth for further instructions.
We’ve drafted a message you can send MexHealth to request your refund or repair — edit it as you like.
Subject: Recall D-0558-2024 — MexHealth MexHealth Hello, I own a MexHealth that is covered by recall D-0558-2024 from MexHealth. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
