FDA recalls MAIN PRODUCTS INC's Umary Acido Hialuronico 850mg caplets due to undeclared Diclofenac and Omeprazole. Stop using immediately as these ingredients are unapproved and potentially harmful.
Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
MAIN PRODUCTS INC is recalling 850mg Umary Acido Hialuronico caplets because they were sold without FDA approval and contain undeclared ingredients that could be harmful. This recall affects consumers who bought these supplements before the expiry date.
The product was sold without FDA approval and contains undeclared Diclofenac and Omeprazole. These ingredients are not approved for use in dietary supplements and could cause health issues, especially if taken without medical supervision.
Anyone who purchased MAIN PRODUCTS INC's Umary Acido: Hialuronico 850mg caplets before the expiry date. People with health conditions requiring careful medication use are at higher risk due to potential interactions with the undeclared ingredients.
Check for 850mg Umary Acido Hialuronico caplets in 30-count bottles. The product was sold with all lots within the expiry date.
Immediately stop using the recalled Umary Acido Hialuronico caplets as they contain undeclared ingredients that could be harmful.
The FDA found that the product was marketed without an approved NDA/ANDA and contains undeclared Diclofenac and Omeprazole.
Stop using it immediately and contact the manufacturer for further instructions.
Yes, the undeclared ingredients could cause health issues, especially for people with health conditions requiring careful medication use.
We’ve drafted a message you can send MAIN PRODUCTS INC to request your refund or repair — edit it as you like.
Subject: Recall D-0626-2024 — MAIN PRODUCTS INC MAIN PRODUCTS INC Hello, I own a MAIN PRODUCTS INC that is covered by recall D-0626-2024 from MAIN PRODUCTS INC. 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.
