|Articles|October 31, 2012

Infusion pump recalled due to malfunctioning touchscreen

The FDA recalled the Symbiq pump touchscreen (Hospira Inc.) on Oct. 29. The screen may not properly respond to user selection, may have a delayed response, or register a value other than the one selected by the user, an FDA press release said.

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Infusion pump recalled due to malfunctioning touchscreen

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