Product Detail

Product Description 5% Dextrose Injection USP,
a) 250 mL (NDC 0409-7922-02),
b) 500 mL (NDC 0409-7922-30),
by Hospira, Inc., Lake Forest, IL 60045

Recall Number D-614-2013

Classification Class II

Code Info Lot #: a) 01-201-JT, Exp 7/12; b) Lot 91-054-JT, Exp 7/12

Product Distributed Qty 267,288 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