Why it was recalled
cGMP deviations.
Product description
fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.
Lot numbers, UPCs & expiration codes
Lot 020226202150202, Exp Date 05/05/2026.
Where it was sold
U.S. Nationwide.
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-0508-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Apr 1, 2026
- FDA report date
- May 6, 2026
- Quantity
- 50 syringes
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Wells Pharma of Houston LLC
Original FDA data
Every field from FDA enforcement report D-0508-2026, exactly as published.
Show all FDA fields
- City
- Houston
- State
- TX
- Status
- Ongoing
- Country
- United States
- Event ID
- 98694
- Address
- 9265 Kirby Dr
- Code information
- Lot 020226202150202, Exp Date 05/05/2026.
- Postal code
- 77054-2520
- Report date
- May 6, 2026
- Product type
- Drugs
- Recall number
- D-0508-2026
- Classification
- Class II
- Recalling firm
- Wells Pharma of Houston LLC
- Product quantity
- 50 syringes
- Reason for recall
- cGMP deviations.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.
- Distribution pattern
- U.S. Nationwide.
- Recall initiation date
- Apr 1, 2026
- Initial firm notification
- Letter
- Center classification date
- Apr 28, 2026