Hospira a Pfizer Company recalls 8.4% Sodium Bicarbonate Inj., USP 50 mL Single-dose, 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL), Rx Only, Mfd by Hospira, I
Recalled August 9, 2017 · FDA recall D-1047-2017 · Hospira a Pfizer
Hazard
Lack of Sterility Assurance · FDA Class II
Units
91,483,150 50 mL single dose vials
Sold at
U.S. (including Puerto Rico), Dutch Antilles, Barbados, Canada, Philippines, Kuwait, and Singapore
Description
Lack of Sterility Assurance
Product
8.4% Sodium Bicarbonate Inj., USP 50 mL Single-dose, 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA, NDC: 0409-6625-02
Manufacturer(s)
Hospira a Pfizer Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →