Recall: Baxter Infusion Pump

The FDA has announced a Class I recall of Baxter Sigma Spectrum Infusion Pumps with Master Drug Library Models No. 35700BAX and 35700ABB, because of incorrect error messages that can interrupt therapy.  For details see http://www.fda.gov/MedicalDevices/Safety/ListofRecalls/ucm395617.htm and http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm395770.htm.

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