HYDROmorphone HCl in 0.9% Sodium Chloride Injection recall: Labeling Error
HYDROmorphone HCl in 0.9% Sodium Chloride Injection, 1 mL Total Volume 1 mg per mL, For IV Use Only, Rx Only, Compounded by: PharMEDium Services LLC.…
Why was HYDROmorphone HCl in 0.9% Sodium Chloride Injection recalled?
Labeling: Incorrect or Missing Lot and/or Exp. Date
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: 172410025C; Exp. 11/27/2017
- Product
- HYDROmorphone HCl in 0.9% Sodium Chloride Injection, 1 mL Total Volume 1 mg per mL, For IV Use Only, Rx Only, Compounded by: PharMEDium Services LLC.…
- Recalling firm
- Pharmedium Services, LLC
- Quantity
- Unknown
- Distribution
- Nationwide.
- Recall date
- January 3, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)