0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-02

Recall Number: D-608-2013

Firm: Hospira Inc.

Classification: Class II

Status: Terminated

Report Date: 20130626

Initiation Date: 20130606

Termination Date: 20150515

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.

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 0409-7983-02