FDA-Drug2013-07-03Class II
0.9% Sodium Chloride Injection, USP, Polyolefin Flexible Container, a) 500 mL (NDC 0409-7983-30), b) 1000 mL (NDC 0409-7983-48), c) 250 mL (NDC 0409-7983-02), d) 150 mL (NDC 0409-7983-61), Rx Only, by 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
2,137,660 units
Manufactured in
275 N Field Dr, Lake Forest, IL, United States
Products
0.9% Sodium Chloride Injection, USP, Polyolefin Flexible Container, a) 500 mL (NDC 0409-7983-30), b) 1000 mL (NDC 0409-7983-48), c) 250 mL (NDC 0409-7983-02), d) 150 mL (NDC 0409-7983-61), Rx Only, by Hospira, Inc., Lake Forest, IL 60045
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-611-2013Don't want to check this manually?
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