FDAClass IIAugust 23, 2017

0.9% Sodium Chloride Injection recall: Particulate Matter

0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09

Why was 0.9% Sodium Chloride Injection recalled?

Presence of Particulate Matter; stainless steel

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: 61-841-FW Exp. 01/01/2018

Product
0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09
Recalling firm
ICU Medical Inc
Quantity
436,716 flexible containers
Distribution
Nationwide
Recall date
August 23, 2017
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls