0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09
Reported: February 27, 2019 Initiated: February 4, 2019 #D-0509-2019
Product Description
0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09
Reason for Recall
CGMP Deviations
Details
- Recalling Firm
- ICU Medical Inc
- Units Affected
- 475320 bags
- Distribution
- Nationwide within the United States
- Location
- LAKE FOREST, IL
Frequently Asked Questions
What product was recalled? ▼
0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09. Recalled by ICU Medical Inc. Units affected: 475320 bags.
Why was this product recalled? ▼
CGMP Deviations
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 27, 2019. Severity: Moderate. Recall number: D-0509-2019.
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