FDAClass ISeptember 4, 2013

0.9% Sodium Chloride Injection recall: Particulate Matter

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

Why was 0.9% Sodium Chloride Injection recalled?

Presence of Particulate Matter; product may contain fibrous material

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
Recalling firm
Hospira Inc.
Quantity
264,432 bags
Distribution
Nationwide
Recall date
September 4, 2013
Classification
Class I
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls