HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride recall: Sterility Concern
HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride Injection, 100 mL Grey CADD Cassette (20 mg/100 mL), CII, Rx only, SCA Pharmaceuticals, 755…
Why was HYDROmorphone HCl 20 mg/100mL 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 #: 1223049529, Exp 01/03/24
- Product
- HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride Injection, 100 mL Grey CADD Cassette (20 mg/100 mL), CII, Rx only, SCA Pharmaceuticals, 755…
- Recalling firm
- SCA Pharmaceuticals, LLC
- Quantity
- 256 cassettes
- Distribution
- Nationwide in the USA
- Recall date
- April 3, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)