Hospira Inc. recalls Sodium Acetate Injection, USP, 40 mEq/20 ml (2 mEq/mL) 20 mL Single-Dose Fliptop, Rx only, HOSPIRA, INC. LAKE FOREST, IL
Recalled May 15, 2013 · FDA recall D-316-2013 · Hospira
Hazard
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial. · FDA Class II
Units
266,900 vials
Sold at
Nationwide and Puerto Rico
Description
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Product
Sodium Acetate Injection, USP, 40 mEq/20 ml (2 mEq/mL) 20 mL Single-Dose Fliptop, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, NDC 0409-7299-73
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →