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-309-2013

Classification Class II

Code Info Lot 17-100-EV and 17-399-EV

Product Distributed Qty 172,350 vials

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

Event Id 64720

Product Type Drugs

Status Ongoing

Recalling Firm Hospira Inc., Lake Forest, IL, US


Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2012-08-28

Initial Firm Notification of Consignee or Public Letter

Distribution Pattern Nationwide and Puerto Rico