Datascope/Getinge has issued a recall of specific Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pumps (IABP) due to a potential shutdown risk from Coiled Cord Connection Failure leading to death. On 03/17/2023, The U.S. FDA classified the recall as a Class I Recall, the most severe type of recall. A Class I Recall means the usage … [Read more...] about Cardiosave Intra-Aortic Balloon Pump Wrongful Death Lawsuit Lawyers