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0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Fores...

FDA Recall #D-922-2013 — Class I — August 31, 2012

Recall #D-922-2013 Date: August 31, 2012 Classification: Class I Status: Terminated

Product Description

0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23

Reason for Recall

Presence of Particulate Matter; product may contain fibrous material

Recalling Firm

Hospira Inc. — Lake Forest, IL

Classification

Class I — Reasonable probability of serious adverse health consequences or death.

Product Type

Drugs

Product Quantity

264,432 bags

Distribution

Nationwide

Code Information

Lot Number 05-201-JT, Expiration Date 1MAY2013

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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