Product Detail

Product Description Diazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, NDC 0409-3213-12

Recall Number D-501-2013

Classification Class II

Code Info 17-099-EV Exp 05/14

Product Distributed Qty 95,700 vials

Reason For Recall Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

Event Detail

Event Id 65315

Product Type Drugs

Status Ongoing

Recalling Firm
Hospira Inc.
City Lake Forest

State IL
Country US

Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2013-05-16

Initial Firm Notification of Consignee or Public Letter

Distribution Pattern Nationwide and Puerto Rico