Intra-Aortic Balloon Pumps by Datascope/MAQUET: Class I Recall - False Blood Detection Alarm, Ingress of Fluid Into Pump
Date of publication: 06-09-2017
If therapy is stopped during use without a replacement IABP available, device failure may result in immediate and serious adverse health consequences, including death. Źródło: https://www.fda.gov
