PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: August 23, 2017 Initiated: July 26, 2017 #D-1091-2017

Product Description

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

Reason for Recall

Presence of Particulate Matter; stainless steel

Details

Recalling Firm
ICU Medical Inc
Units Affected
436,716 flexible containers
Distribution
Nationwide
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09. Recalled by ICU Medical Inc. Units affected: 436,716 flexible containers.
Why was this product recalled?
Presence of Particulate Matter; stainless steel
Which agency issued this recall?
This recall was issued by the FDA Drug on August 23, 2017. Severity: Moderate. Recall number: D-1091-2017.