FDA-Drug2013-04-10Class II
0.9% Sodium Chloride Injection, USP, 50 mL, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7984-36 Hospira, Inc., Lake Forest, IL 60045
Hospira Inc.
Hazard
Lack of Assurance of Sterility: The product is being recall due to the product lot being incorrectly released without meeting product specifications. There is the potential for the solution to leak from the administrative port to the fill tube seal.
Sold states
Nationwide
Affected count
624,240 units
Manufactured in
275 N Field Dr, N/A, Lake Forest, IL, United States
Products
0.9% Sodium Chloride Injection, USP, 50 mL, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7984-36 Hospira, Inc., Lake Forest, IL 60045
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-243-2013Don't want to check this manually?
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