Hydromorphone Hydrochloride Injection recall: Particulate Matter
Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial per Carton, 100 vials per case. Hospira, Inc., Lake…
Why was Hydromorphone Hydrochloride Injection recalled?
Presence of Particulate Matter: Silicone oil
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 #: 56260DD, Exp. 01AUG2017
- Product
- Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial per Carton, 100 vials per case. Hospira, Inc., Lake…
- Recalling firm
- HOSPIRA INC, LAKE FOREST
- Quantity
- 9,009 vials
- Distribution
- Nationwide in the USA
- Recall date
- August 16, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)