FDAClass IMay 13, 2015

0.9% Sodium Chloride Injection recall: Particulate Matter

0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.

Why was 0.9% Sodium Chloride Injection recalled?

Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.

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 # 45-110-C6; Exp 03/1/16

Product
0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.
Recalling firm
Hospira Inc.
Quantity
9,912 VisIV flex containers
Distribution
Nationwide.
Recall date
May 13, 2015
Classification
Class I
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls