Product Detail

Product Description 20% Dextrose Injection, USP,
a) 500 mL in 1000 mL Partial-Fill Container (NDC 0409-7935-19),
b) 500 mL VisIV Container (NDC 0409-7953-30),
c) 1000 mL VisIV Container, (NDC 0409-7953-48),
Rx Only, Hospira, Inc., Lake Forest, IL 60045

Recall Number D-616-2013

Classification Class II

Code Info Lot #:
a) 09-183-JT, Exp 3/13;
b) 01-081-JT, Exp 7/12;
c) 07-078-JT, 91-083-JT, Exp 7/12

Product Distributed Qty 216,396 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