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 ...
Medscape

FDA Warns of Possible Maquet/Datascope IABP Battery Failure

Maquet/Datascope intra-aortic balloon pumps (IABPs) may be at risk of shutting down while running on batteries, failure of their batteries to charge, or premature battery depletion, the US Food and ...
TCTMD

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

(UPDATED) The Cardiosave Hybrid and Cardiosave Rescue intra-aortic balloon pumps (IABPs) have been placed under recall by the manufacturer (Getinge/Datascope/Maquet) following reports of fluid leaks, ...
Healio

FDA designates recall of two intra-aortic balloon pumps as class I

Please provide your email address to receive an email when new articles are posted on . Datascope/Maquet/Getinge intra-aortic balloon pumps recalled due to risk for unexpected shutdown. The FDA has ...
Business Wire

MAQUET Medical Systems USA Showcases CARDIOSAVE®™ IABP HYBRID & RESCUE at National Event Committed to Healthcare Innovation

WAYNE, N.J.--(BUSINESS WIRE)--CARDIOSAVE ® IABP HYBRID & RESCUE was one of 14 medical innovations on display in front of thousands of healthcare providers and experts at the Premier healthcare ...
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 ...
HealthLeaders Media

FDA warns of ‘continued safety and quality concerns’ in Getinge recalls

The warning covers Getinge/Maquet/Datascope Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pump (IABP) devices and the Getinge/Maquet Cardiohelp system and HLS sets ...
BioWorld

Maquet wins panel support for IABP reclassification

Maquet Cardiovascular (Wayne, New Jersey), a provider of intra-aortic balloon (IAB) therapy devices, reported this week that the Circulatory System Devices Panel of the FDA recently voted to support ...
Becker's Hospital Review

2 more deaths, 60 device failures linked to Getinge’s heart balloon pump

Two deaths, one serious injury and more than 60 medical device reports have been linked to Maquet/Datascope’s intra-aortic balloon pumps in the past year, the FDA warned healthcare providers in a Nov.
MD&M East

Maquet Intra-Aortic Balloon Pumps

Some of the intra-aortic balloon pumps (IABP) made by Maquet Datascope Corporation were recalled in March 2014 because the device's fan assembly could malfunction and cause the device to stop with any ...
Healio

Hybrid intra-aortic balloon pump recalled

The FDA announced that Maquet Datascope Corp. has recalled a hybrid intra-aortic balloon pump due to a design issue that allows fluid, such as saline, to seep into the device. The agency designated ...
Business Insider

Datascope Moves To Join Maquet's Patent Infringement Case Against Abiomed In Order To Add False Advertising Claims

WAYNE, N.J., June 16, 2017 /PRNewswire/ -- Datascope Corp. today announced the filing of a motion to join Maquet Cardiovascular LLC's existing patent infringement case against Abiomed, Inc. in the ...