0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
Reported: August 14, 2013 Initiated: March 29, 2013 #D-836-2013
Product Description
0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
Reason for Recall
Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 691,356 containers
- Distribution
- Nationwide
- 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, NDC 0409-7983-09.. Recalled by Hospira Inc.. Units affected: 691,356 containers.
Why was this product recalled? ▼
Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 14, 2013. Severity: Critical. Recall number: D-836-2013.
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