Product Detail

Product Description 0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC

Recall Number D-608-2013

Classification Class II

Code Info Lot #: 16-031-JT*, Exp 1APR2014; Note the * may be followed by 01 or 02

Product Distributed Qty 676,872 containers

Reason For Recall Lack of Assurance of Sterility: The product has the potential for solution to leak at or near the administrative port of the primary container.

Event Detail

Event Id 65400

Product Type Drugs

Status Ongoing

Recalling Firm
Hospira Inc.
City Lake Forest

State IL
Country US

Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2013-06-06

Initial Firm Notification of Consignee or Public Letter

Distribution Pattern Nationwide and Puerto Rico