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 c…

Recall date

July 26, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-1081-2017

FDA classification

Class II

Brand / firm

HOSPIRA INC, LAKE FOREST

Sold / distributed

Nationwide in the USA

Why it was recalled

Presence of Particulate Matter: Silicone oil

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What 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