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
Reported: August 16, 2017 Initiated: July 26, 2017 #D-1080-2017
Product Description
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
Details
- Recalling Firm
- HOSPIRA INC, LAKE FOREST
- Units Affected
- 14,300 vials
- Distribution
- Nationwide in the USA
- Location
- LAKE FOREST, IL
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by HOSPIRA INC, LAKE FOREST. Units affected: 14,300 vials.
Why was this product recalled? ▼
Presence of Particulate Matter: Silicone oil
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 16, 2017. Severity: Moderate. Recall number: D-1080-2017.
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