Related topics: Packaging
Hospira has initiated a voluntary recall of one lot of its sodium chloride injection, USP as an incorrect barcode label meant medication errors could occur.
The lot may have been labeled as 5% Dextrose Injection, USP and consequently could be administered incorrectly.
Potential adverse events include electrolyte imbalance, cardiac dysfunction, gastrointestinal disturbances, paresthesia and mental confusion.
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