资讯

health.economictimes.indiatimes1 年
Teleflex Inflatable Devices Recall: US FDA classifies recall of ...
Teleflex Inflatable Devices Recall: The regulator said the company recalled 16,959 of its Arrow FiberOptix Intra-Aortic Balloon Catheter Kits and Arrow UltraFlex Intra-Aortic Balloon Catheter Kits ...
Healio1 年
Two intra-aortic balloon catheter kits recalled; three deaths ... - Healio
If the intra-aortic balloon becomes overtwisted, it may cause blood loss, artery perforation, hemodynamic instability, myocardial ischemia or death, according to an alert from the FDA.