FDAMarch 8, 2016drug

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

What to do

FDA enforcement status: Terminated

Brands named

hospira

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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