fentaNYL Citrate Injectable Solution in 0.9% Sodium recall: CGMP Deviations
fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.
Why was fentaNYL Citrate Injectable Solution in 0.9% Sodium recalled?
cGMP deviations.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot 020226202150202, Exp Date 05/05/2026.
- Product
- fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.
- Recalling firm
- Wells Pharma of Houston LLC
- Quantity
- 50 syringes
- Distribution
- U.S. Nationwide.
- Recall date
- May 6, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)