Hospira Inc. recalls Potassium Chloride Injection 20 mEq, 400 mEq/L, Packaged in 50 mL Bags, Rx only, Hospira, Inc., Lake Forest, IL 60045,…
- Recall date
- March 8, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0832-2016
- FDA classification
- Class II
- Brand / firm
- Hospira Inc.
- Sold / distributed
- US: Nationwide and Singapore
Why it was recalled
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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
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