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 ...
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 ...
FiercePharma

--Study Results Demonstrating Trend Toward Improvement in 30-Day All-Cause Mortality Presented at ESC Congress 2012-

MUNICH and WAYNE, N.J., Aug. 27, 2012 /PRNewswire/ -- MAQUET Cardiovascular LLC, the market leader in intra-aortic balloon counterpulsation therapy, today announced 30-day results from the large, ...
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

New Recall for Maquet/Datascope IABPs Due to Potential Battery Failure

Getinge is recalling numerous Maquet/Datascope intra-aortic balloon pumps (IABPs) due to potential battery failure during use that can lead to unexpected stopping and shortened run times.
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 ...
Healio

Hybrid intra-aortic balloon pump recalled

Please provide your email address to receive an email when new articles are posted on . The FDA announced that Maquet Datascope Corp. has recalled a hybrid intra-aortic balloon pump due to a design ...
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 ...
FierceBiotech

Study: Intra-aortic balloon pumps show little help, possible increase in mortality in worst cases

A Japanese study of intra-aortic balloon pumps appears to indicate the devices do little to improve outcomes for patients with acute cases and may increase the chances of death. In the registry study ...
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 ...
Healio

IABP-SHOCK II: IABP failed to reduce 30-day mortality in patients with cardiogenic shock

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Becker's ASC

MAQUET Cardiovascular Receives FDA Clearance for Intra-Aortic Balloon Catheter

MAQUET Cardiovascular has announced it has received FDA clearance for a new intra-aortic balloon catheter, according to a news release. The SENSATION PLUS 7.5Fr. 40cc IAB catheter is designed to allow ...