Product Detail

Product Description Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Vial, C-IV, Rx Only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-3213-12

Recall Number D-927-2013

Classification Class II

Code Info Lot: 23-505-EV, Exp. 11/14

Product Distributed Qty 72,300 vials

Reason For Recall Lack of assurance of sterility: ineffective crimp on fliptop vials that may result in leaking at the neck of the vials.

Event Detail

Event Id 66104

Product Type Drugs

Status Ongoing

Recalling Firm

Hospira Inc.
City Lake Forest
State IL
Country US

Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2013-08-16

Initial Firm Notification of Consignee or Public Letter

Distribution Pattern Nationwide and Puerto Rico