https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/getingemaquetdatascope-recalls-cardiosave-hybrid-and-rescue-intra-aortic-balloon-pumps-iabps
Getinge/Maquet/Datascope Recalls Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs)...
Cardiosave IABPs are used to inflate and deflate intra-aortic balloons. The device may stop unexpectedly due to Autofill Failure Alarms and will be put in...
intra aortic balloon pumps
https://www.cochrane.org/de/evidence/CD004472_preoperative-intra-aortic-balloon-pumps-patients-undergoing-coronary-artery-bypass-grafting
Preoperative intra aortic balloon pumps in patients undergoing coronary artery bypass grafting |...
intra aortic balloon pumpscoronary artery bypass
https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/datascopegetinge-recalls-certain-cardiosave-hybrid-and-rescue-intra-aortic-balloon-pumps-iabp-risk
Datascope/Getinge Recalls Certain Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pumps (IABP)...
The coiled cord on some Cardiosave IABPs may fail and cause an unexpected shutdown, interrupting therapy to the patient with no warning.
intra aortic balloon pumps
https://www.prweb.com/releases/fda_announces_class_i_recall_of_maquet_datascope_intra_aortic_balloon_pumps_attorneyone_monitor_and_keep_consumers_informed/prweb11888835.htm
FDA Announces Class I Recall of Maquet Datascope Intra-Aortic Balloon Pumps: AttorneyOne Monitor...
San Diego, CA (PRWEB) May 28, 2014 -- AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the...
intra aortic balloon pumps