Drug recall D-1080-2017
Product
Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial. Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618 USA. NDC: 0703-0018-01
Reason for recall
Presence of Particulate Matter: Silicone oil
Lots and codes
Lot #: 560053F, Exp. 01AUG2017
Recall details
- Recalling firm
- HOSPIRA INC, LAKE FOREST, LAKE FOREST, IL
- Quantity
- 14,300 vials
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 26, 2017
- Terminated
- May 11, 2018
Related products
- Hydromorphone Hydrochloride – drug information
- NDC 0703-0113 Hydromorphone Hydrochloride · Hydromorphone Hydrochloride 10 mg/mL · Teva Parenteral Medicines, Inc.
- NDC 0703-0018 Hydromorphone Hydrochloride · Hydromorphone Hydrochloride 10 mg/mL · Teva Parenteral Medicines, Inc.
- NDC 0703-0110 Hydromorphone Hydrochloride · Hydromorphone Hydrochloride 10 mg/mL · Teva Parenteral Medicines, Inc.