HYDROmorphone in 0.9% sodium chloride recall: Sterility Concern
HYDROmorphone in 0.9% sodium chloride, 10 mg/50 mL, (0.2 mg/mL), 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook…
Why was HYDROmorphone in 0.9% sodium chloride recalled?
Lack of assurance of sterility:
What should I do if I have this product?
Review the official FDA enforcement record for current 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:17-275728, Exp. 10/9/2023; 17-275791, 17-275803, Exp. 10/10/2023; 17-276244, Exp. 10/20/2023.
- Product
- HYDROmorphone in 0.9% sodium chloride, 10 mg/50 mL, (0.2 mg/mL), 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook…
- Recalling firm
- Central Admixture Pharmacy Services Inc
- Quantity
- 1,190 50 mL syringes
- Distribution
- Nationwide in the USA
- Recall date
- October 11, 2023
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)