Why it was 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.
Product description
UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323
Lot numbers, UPCs & expiration codes
Lot#: 24183, Exp 07/01/28
Where it was sold
Product was sold via Amazon Marketplace.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0166-2025
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Nov 14, 2024
- FDA report date
- Jan 1, 2025
- Quantity
- 321 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- MXBBB
Original FDA data
Every field from FDA enforcement report D-0166-2025, exactly as published.
Show all FDA fields
- City
- El Paso
- State
- TX
- Status
- Ongoing
- Country
- United States
- Event ID
- 95777
- Address
- 1162 Tio Dink Cir
- Code information
- Lot#: 24183, Exp 07/01/28
- Postal code
- 79907-1912
- Report date
- Jan 1, 2025
- Product type
- Drugs
- Recall number
- D-0166-2025
- Classification
- Class II
- Recalling firm
- MXBBB
- Product quantity
- 321 bottles
- 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.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- UMARY ACID HYALURONIC, 850 MG CAPLETS, 30-count bottle, UPC7502265120323
- Distribution pattern
- Product was sold via Amazon Marketplace.
- Recall initiation date
- Nov 14, 2024
- Initial firm notification
- Press Release
- Center classification date
- Dec 26, 2024