Hospira Issues Voluntary Recall of One Lot of 20meq Potassium Chloride in 5 Percent Dextrose and 0.45 Percent Sodium Chloride Injection, USP Due to Incorrect Bar Code Label (December 8)

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Title: Hospira Issues Voluntary Recall of One Lot of 20meq Potassium Chloride in 5 Percent Dextrose and 0.45 Percent Sodium Chloride Injection, USP Due to Incorrect Bar Code Label (December 8)

Hospira Issues Voluntary Recall of One Lot of 20meq Potassium Chloride in 5 Percent Dextrose and 0.45 Percent Sodium Chloride Injection, USP Due to Incorrect Bar Code Label (December 8)
Tue, 09 Dec 2008 05:53:00 -0600

The incorrect bar code could lead to a medication error resulting in the wrong drug being delivered to a patient if a bar code system is used to confirm the medication. Potential adverse events related to an error of this type include electrolyte imbalance, cardiac dysfunction, gastrointestinal disturbances, paresthesia and mental confusion.


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