HOSPIRA INC, LAKE FOREST recalls Hydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial.(10 vials per carton NDC 0703-0
Recalled August 16, 2017 · FDA recall D-1082-2017 · HOSPIRA INC, LAKE FOREST
Hazard
Presence of Particulate Matter: Silicone oil · FDA Class II
Units
56,340 vials
Sold at
Nationwide in the USA
Description
Presence of Particulate Matter: Silicone oil
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 (NDC 0703-0113-03) Mfd By: Hospira, Inc., Lake Forest, IL 60045 USA, Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618 USA.
Manufacturer(s)
HOSPIRA INC, LAKE FOREST
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →