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 of the devices since March 6, 2012. At the time of the recall, the company had reported 134 complaints, including 12 device … [Read more...] about Datascope/Getinge Recalls Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pumps