HOSPIRA INC, LAKE FOREST recalls Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial per Carton, 100 vials per ca
Recalled August 16, 2017 · FDA recall D-1081-2017 · HOSPIRA INC, LAKE FOREST
Hazard
Presence of Particulate Matter: Silicone oil · FDA Class II
Units
9,009 vials
Sold at
Nationwide in the USA
Description
Presence of Particulate Matter: Silicone oil
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 Forest, IL 60045 USA, NDC: 0409-2634-50
Manufacturer(s)
HOSPIRA INC, LAKE FOREST
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →