Hydromorphone recall: Sterility Concern
Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Hospira, Inc., Lake forest, IL…
Why was Hydromorphone recalled?
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
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 71330DD EXP. 11/1/2018.
- Product
- Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Hospira, Inc., Lake forest, IL…
- Recalling firm
- Pfizer Inc.
- Quantity
- 29, 680 vials
- Distribution
- Nationwide in the USA
- Recall date
- March 21, 2018
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)