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 Forest, IL 60045 USA, NDC: 0409-2634-50
Reported: August 16, 2017 Initiated: July 26, 2017 #D-1081-2017
Product Description
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 Forest, IL 60045 USA, NDC: 0409-2634-50
Reason for Recall
Presence of Particulate Matter: Silicone oil
Details
- Recalling Firm
- HOSPIRA INC, LAKE FOREST
- Units Affected
- 9,009 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 per Carton, 100 vials per case. Hospira, Inc., Lake Forest, IL 60045 USA, NDC: 0409-2634-50. Recalled by HOSPIRA INC, LAKE FOREST. Units affected: 9,009 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-1081-2017.
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