FDA-Drug2013-07-03Class II
0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984-13), b) 50 mL (NDC 0409-7984-36), c) 100 mL (0409-7984-37), Rx Only, Hospira, Inc., Lake Forest, IL 60045
Hospira Inc.
Hazard
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
Sold states
Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia
Affected count
2,933,936 units
Manufactured in
275 N Field Dr, Lake Forest, IL, United States
Products
0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984-13), b) 50 mL (NDC 0409-7984-36), c) 100 mL (0409-7984-37), Rx Only, Hospira, Inc., Lake Forest, IL 60045
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-619-2013Don't want to check this manually?
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