HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride recall: Sterility Concern
HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR…
Why was HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride recalled?
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
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: 9016 BUD: 3/7/2017
- Product
- HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR…
- Recalling firm
- Cantrell Drug Company
- Quantity
- 935 syringes
- Distribution
- Nationwide
- Recall date
- December 21, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)