FDA-Drug2013-07-03Class II
5% Dextrose Injection USP, a) 250 mL (NDC 0409-7922-02), b) 500 mL (NDC 0409-7922-30), 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
267,288 units
Manufactured in
275 N Field Dr, Lake Forest, IL, United States
Products
5% Dextrose Injection USP, a) 250 mL (NDC 0409-7922-02), b) 500 mL (NDC 0409-7922-30), by Hospira, Inc., Lake Forest, IL 60045
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-614-2013Don't want to check this manually?
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