(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, ...

Alert Another FDA Class I Recall of Cardiosave Hybrid/Rescue IABPs The 4586 recalled Cardiosave Hybrid/Rescue intra-aortic balloon pumps may shutdown unexpectedly due to electrical failures in the ...

The recall includes a total of 2300 CardioSave Hybrid or Rescue IABP units distributed prior to July 24, 2017, and/or coiled cord part number 0012-00-1801.

Cardiosave Hybrid and Cardiosave Rescue intra-aortic balloon pumps (IABPs) manufactured by Getinge/Datascope are being recalled due to the possibility that a coiled cable connecting the display and ...

About 16,000 of Getinge’s Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps have been recalled in 2023, according to the FDA. Advertisement. By: Paige Twenter. Friday, August 18th, 2023.

The FDA on Jan. 25 announced a class 1 recall of Datascope/Getinge's Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pump after one death and four serious injuries were reported.

MAQUET Medical Systems USA’s CARDIOSAVE ® ™ IABP HYBRID & RESCUE device was selected by clinicians and other members of Premier, a provider-owned performance improvement alliance of more than ...

The recall affects just over 8,900 of the Hybrid and Rescue models of Getinge's Cardiosave balloon pumps, half of which were distributed in the U.S.

In a flurry of Aug. 31 notices from the FDA, the number of Class I recalls plaguing Getinge’s Cardiosave intra-aortic balloon pumps this year has doubled.

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 ...