Home › Over-the-counter & supplements › MAIN PRODUCTS INC — Umary Acido Hialuronico,…
MAIN PRODUCTS INC — Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.
Stop taking it and tell your doctor or pharmacist.
Why this is on The Recall Registry: This is a consumable product recalled for what is inside it. It was found to contain a drug or chemical that is not on the label. That is different from an allergen or a contamination scare: anyone taking it has been taking a substance nobody prescribed, in an unknown dose, and it can interact with medication they are already on. Follow the agency notice rather than judging it by how the product looks.
What’s wrong
Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
The Recall Registry rates this highest risk — FDA Class I: reasonable probability of serious harm or death.
What to do
Stop taking it, and tell your doctor or pharmacist that you have been taking it. It contains a drug ingredient that is not on the label, so they need to know — it can interact with medication you are already on.
Who to contact: Recalling firm: MAIN PRODUCTS INC
The product
Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.
Details
- Units affected
- 57, 340 bottles
- Recall date
- July 18, 2024
- Brand
- MAIN PRODUCTS INC
Nationwide within the U.S
The official notice
This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.
Their exact wording: “MAIN PRODUCTS INC — Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.”
Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.
Filed under: Over-the-counter & supplements