Hospira Inc. recalls Potassium Chloride Injection 20 mEq, 400 mEq/L, Packaged in 50 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045,
Recalled April 27, 2016 · FDA recall D-0832-2016 · Hospira
Hazard
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin. · FDA Class II
Units
81888 bags
Sold at
US: Nationwide and Singapore
Description
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Product
Potassium Chloride Injection 20 mEq, 400 mEq/L, Packaged in 50 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7077-14
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →