Hospira Symbiq Infusion System Touchscreen: Class I Recall - May Not Respond to Selection
MedSun: Newsletter #78, November 2012

FDA MedWatch Safety Alert

These devices may not respond to user selection, may experience a delayed response or may register a different value from the value selected by the user. Failure of the touchscreen to respond to user input could result in a delay or interruption in therapy or over delivery or under delivery of medication if the user does not confirm the programmed values on the pump's confirmation screen before starting the infusion. All serial numbers for these models are affected by this recall.

Additional Information:

Hospira Symbiq Infusion System Touchscreen: Class 1 Recall - May Not Respond to Selection. FDA MedWatch Safety Alert. October 29, 2012.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm326080.htm


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