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.
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