Hospira a Pfizer Company recalls Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial carto
Recalled August 9, 2017 · FDA recall D-1049-2017 · Hospira a Pfizer
Hazard
Lack of Sterility Assurance · FDA Class II
Units
21,436,700 5mL single dose vials
Sold at
U.S. (including Puerto Rico), Dutch Antilles, Barbados, Canada, Philippines, Kuwait, and Singapore
Description
Lack of Sterility Assurance
Product
Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial carton (NDC 0409-6609-25), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA
Manufacturer(s)
Hospira a Pfizer Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →