Hydromorphone Hydrochloride Injection recall: Particulate Matter
Hydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial.(10 vials per carton NDC 0703-0113-01) and 180 vials per case…
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 #: 560103F, Exp. 01AUG2017
- Product
- Hydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial.(10 vials per carton NDC 0703-0113-01) and 180 vials per case…
- Recalling firm
- HOSPIRA INC, LAKE FOREST
- Quantity
- 56,340 vials
- Distribution
- Nationwide in the USA
- Recall date
- August 16, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)