CLASS II ONGOING Drug recall · Reported 1 Jan 2025 · FDA Enforcement Report
Umary Acid Hyaluronic, 850 MG Caplets, Upc7502265120323 recalled
Mxbbb is recalling Umary Acid Hyaluronic, 850 MG Caplets, Upc7502265120323. The recall was initiated on 14 Nov 2024 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0166-2025
- FDA event ID
- 95777
- Recalling firm
- Mxbbb, El Paso, TX
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 14 Nov 2024
- FDA classified
- 26 Dec 2024
- Reported
- 1 Jan 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 14 Nov 2024 | Recall initiated by company | |
| 26 Dec 2024 | Classified by FDA | +42 days |
| 1 Jan 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
cGMP Deviations: the firm initiated a recall after notification from the distributor that product may be tainted with undeclared diclofenac and omeprazole, however there is no analytical data confirming that product distributed by the firm is tainted.
Product as listed by the FDA
UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323
Where it was distributed
Product was sold via Amazon Marketplace.
Stores named: Amazon, Online Retailers
Questions about this recall
Why was it recalled?
cGMP Deviations: the firm initiated a recall after notification from the distributor that product may be tainted with undeclared diclofenac and omeprazole, however there is no analytical data confirming that product distributed by the firm is tainted.
Which lots are affected?
Lot#: 24183, Exp 07/01/28
Where was it sold?
Product was sold via Amazon Marketplace.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.