Datascope Corp.
15 Law Drive
Fairfield
NJ
07004
U.S.
+1 973 244 6100
+1 973 244 6279
http://www.datascope.com

Datascope Corp. is currently merging with MAQUET Cardiovascular LLC.

Product Categories
Cardiovascular Surgery, Angiography

Related Content

The FDA has announced that Datascope/Maquet/Getinge is recalling the Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) because they may shutdown unexpectedly due to electrical failures in the Power Management Board and/or Solenoid Board (Power Source Path).
News | Intra-Aortic Balloon Pumps (IABP)
Datascope/Maquet/Getinge Recalls Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps (IABPs) for Unexpected Shutdowns

August 14, 2023 — The FDA has announced that Datascope/Maquet/Getinge is recalling the Cardiosave Hybrid and Rescue ...

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According to a new release issued by the U.S. Food and Drug Administration (FDA), Datascope, a subsidiary of Getinge, is recalling Cardiosave Hybrid IABPs and Rescue IABPs because a communication loss between the executive processor printed circuit board assembly (PCBA) and the video generator PCBA may cause an unexpected shutdown
News | Intra-Aortic Balloon Pumps (IABP)
Datascope/Getinge Issues New Recall of Certain Cardiosave Hybrid and Rescue IABPs for Risk of Unexpected Shutdown

March 31, 2023 — According to statement issued by the U.S. Food and Drug Administration (FDA), Datascope, a subsidiary ...

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Datascope, a subsidiary of Getinge, is recalling Cardiosave Hybrid IABPs and Rescue IABPs because the coiled cable connecting the display and base on some units may fail, causing an unexpected shutdown
News | Intra-Aortic Balloon Pumps (IABP)
Datascope/Getinge Recalls Certain Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pumps (IABP) for Risk of Unexpected Shutdown After Coiled Cord Connection Failure

March 20, 2023 — According to a statement issued by the U.S. Food and Drug Administration (FDA), Datascope, a subsidiary ...

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Since Maquet/Datascope first recalled all of its intra-aortic balloon pumps (IABP) due to reports of the batteries failing in November 2018, a year later the U.S. Food and Drug Administration said its has received more than 60 additional medical device reports related to this issue. These included two patient deaths and one serious patient injury.
News
Over 60 New Safety Reports Filed With FDA for Maquet IABPs Turning Off During Use

November 19, 2019 — Since Maquet/Datascope first recalled all of its intra-aortic balloon pumps (IABP) due to reports of ...

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Datascope Recalls Intra-Aortic Balloon Pumps Due to Potential Battery Failure. FDA Class I recall includes the Cardiosave Hybrid, Cardiosave Rescue, CS300 and CS100/100i IABP.
Feature | Intra-Aortic Balloon Pumps (IABP)
Datascope Recalls Intra-Aortic Balloon Pumps Due to Potential Battery Failure

July 24, 2019 — The U.S. Food and Drug Administration announced Maquet/Datascope is recalling all intra-aortic balloon ...

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he U.S. Food and Drug Administration (FDA) is evaluating recent reports of Getinge's Maquet/Datascope intra-aortic balloon pump (IABP) devices shutting down while running on battery power.
News | Intra-Aortic Balloon Pumps (IABP)
Maquet/Datascope Intra-Aortic Balloon Pumps Might Fail on Battery Power

November 5, 2018 — The U.S. Food and Drug Administration (FDA) is evaluating recent reports of Getinge's Maquet ...

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Maquet Datascope Corp. is recalling the CardioSave Hybrid Intra-aortic Balloon Pump (IABP).
News | Intra-Aortic Balloon Pumps (IABP)
FDA Class 1 Recall of Maquet Datascope IABPs Due to Fluid Seepage

June 6, 2018 — Maquet Datascope Corp. said it is recalling the CardioSave Hybrid Intra-aortic Balloon Pump (IABP) due to ...

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IABP recall for Maquet, Datascope intra-aortic balloon pump CS100 and CS300
News | Hemodynamic Support Devices
FDA Announces Recall of Maquet Intra-aortic Balloon Pumps

June 20, 2017 — The U.S. Food and Drug Administration (FDA) said Maquet/Datascope is voluntarily performing a worldwide ...

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hemostasis management cath lab safeguard medical systems datascope air-band
Technology
Merit Medical Acquires Hemostatic Devices From Datascope

October 7, 2013 — Merit Medical Systems Inc. announced that it has acquired Datascope Corp.’s Safeguard Pressure ...

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Technology
CS100 Intra-Aortic Balloon Pump Adapts to Changing Patient Conditions

Datascope’s CS100 Intra-Aortic Balloon Pump with IntelliSync offers one-button start up and it automatically adapts to ...

Home October 14, 2009
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