HYDROmorphone HCl in Sodium Chloride 0.9% in all doses recall: Sterility Concern
HYDROmorphone HCl in Sodium Chloride 0.9% in all doses, all strengths, and all packaging.
Why was HYDROmorphone HCl in Sodium Chloride 0.9% in all doses recalled?
Lack of sterility assurance.
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?
All lots remaining within expiry.
- Product
- HYDROmorphone HCl in Sodium Chloride 0.9% in all doses, all strengths, and all packaging.
- Recalling firm
- Pharmedium Services, LLC
- Quantity
- Unknown
- Distribution
- U.S.A. Nationwide
- Recall date
- February 28, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)