Product Detail

Product Description 5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-48

Recall Number D-615-2013

Classification Class II

Code Info Lot #: 11-161-JT, Exp 11/13

Product Distributed Qty 74,256 units

Reason For Recall Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Event Detail

Event Id 61918

Product Type Drugs

Status Ongoing

Recalling Firm
Hospira Inc.
City Lake Forest

State IL
Country US

Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2012-05-04

Initial Firm Notification of Consignee or Public Letter

Distribution Pattern Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia