D-1081-2017 Class II Terminated

Recalled by HOSPIRA INC, LAKE FOREST — LAKE FOREST, IL

Recall Details

Product Type
Drugs
Report Date
August 16, 2017
Initiation Date
July 26, 2017
Termination Date
May 11, 2018
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
9,009 vials

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

Distribution Pattern

Nationwide in the USA

Code Information

Lot #: 56260DD, Exp. 01AUG2017