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Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

The beleaguered company is pulling the pumps due to electrical failures in the power management or solenoid boards.

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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 power source path, leading to serious harm.

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10 biggest medical device recalls in 2023

Get the scoop on the 10 biggest medical device recalls of the first half of 2023, from drug delivery devices to body scanners and breathing circuits.

Philips respironicsHealth hazard assessmentNuclear medicineAkorn operating coGe healthcareTeva pharmaceuticalsAirway pressureSmiths medicalContinuous ambulatory delivery deviceCardiosave hybridFreestyle libreKabi united statesSeattle positive airway pressure plus

11 device, medication recalls for ASC leaders to know

Stay up-to-date on the latest device and medication recalls since March 23 with this list of 11 important recalls for health leaders to know.

Airway pressureAkorn operating coTeva pharmaceuticalsCamber pharmaceuticalsSeattle positive airway pressure plusKabi united statesCardiosave hybridDevice recallsMedication recallsBacterial contaminationEye dropsCardiosave hybrid

Intra-Aortic Balloon Pumps (IABP)

This channel includes news and new technology innovations for intra-aortic balloon pumps (IABP). IABPs are a type of hemodynamic support device that is inserted into the aorta to help augment the flow of blood with a pulsing balloon that pushes the blood volume out of the the aorta to help perfuse organs and tissues.

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