Intra-Aortic Balloon Pumps by Datascope/MAQUET: Class I Recall - False Blood Detection Alarm, Ingress of Fluid Into Pump

By Newsroom America Feeds at 6 Sep 2017

If therapy is stopped during use without a replacement IABP available, device failure may result in immediate and serious adverse health consequences, including death.

https://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm574893.htm

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