Product Detail

Product Description 0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984-13), b) 50 mL (NDC 0409-7984-36), c) 100 mL (0409-7984-37), Rx Only, Hospira, Inc., Lake Forest, IL 60045

Recall Number D-619-2013

Classification Class II

Code Info Lot #: a) 11-085-JT, Exp 11/13; b) 06-111-JT, Exp 12/12, c) 93-030-JT, 14-044-JT, Exp 9/12

Product Distributed Qty 2,933,936 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