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Critical recall: Death or serious injury has been reported or is considered likely. Stop using this product now.

SoloVital 2024-08-07 Health critical FDA
Health · FDA · Recall #FDA-D-0620-2024

Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count… Recall

Issued August 7, 2024 · SoloVital

In August 2024, SoloVital recalled the Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.

What you should do

  1. 1 Stop using Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact SoloVital to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
SoloVital
Category
Health
Recall date
August 7, 2024
Units affected
Not reported
Sold at
Nationwide within the United States
Recall number
FDA-D-0620-2024
Made in
United States
Issuing agency
FDA

In context

  • SoloVital has 1 recall in our database, including 1 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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