TCTMD

Maquet Recalls Intra-Aortic Balloon Pumps Due to Potential Failure of Power Supply

— Datascope Corp./Maquet initiated a voluntary worldwide field correction of some of its intra-aortic balloon pumps (IABPs) due to a potential mechanical failure of the fan assembly associated with ...
TCTMD

Recall Underway for Certain IABPs Due to Potential Electrical Test Failure

Datascope/Maquet have initiated a worldwide recall of certain intra-aortic balloon pump (IABP) systems to address potential electrical test failures. The action involves CS100, CS100i, and CS300 IABPs ...
Medscape

Global Recall for Maquet/Datascope Intra-aortic Balloon Pumps

Maquet/Datascope is recalling all intra-aortic balloon pumps (IABPs) after reports of the batteries failing to hold a charge, stopping unexpectedly, and having a shortened run-time, according to the ...
Medscape

FDA Update on Maquet/Datascope Intra-aortic Balloon Pump Failures

The US Food and Drug Administration (FDA) continues to receive reports of device failures associated with Maquet/Datascope Cardiosave Hybrid, Cardiosave Rescue, CS300, and CS100/CS100i intra-aortic ...
RAPS

Five Deaths Reported Prior to Recall of Intra-aortic Balloon Pumps

The US Food and Drug Administration (FDA) on Tuesday designated Getinge’s Maquet/Datascope recall of intra-aortic balloon pumps (IABPs) as Class I after five patient deaths were reported since 2016.