Datascope/Getinge Recalls Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pumps
On January 25, 2023, the U.S. Food and Drug Administration (FDA) announced that Datascope is recalling its Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) and Rescue IABPs. Datascope had distributed 4,454 [...]