Another FDA Class I Recall of Cardiosave Hybrid/Rescue IABPs
The 4586 recalled Cardiosave Hybrid/Rescue intra-aortic balloon pumps may shutdown unexpectedly due to electrical failures in the power source path, leading to serious harm.
Datascope Maquet Getinge Datascope Getinge Cardiosave Iabps Drug Administration Cardiosave Hybrid Rescue Intra Aortic Balloon Pumps
Source: medscape.com