Medtronic PLC is discontinuing all implants of one of its most complex and costly heart-failure devices, the HeartWare Ventricular Assist Device, five years after the Minnesota device maker acquired the HVAD's maker in a $1.1 billion deal.
Medtronic and the U.S. Food and Drug Administration announced Thursday that the device should no longer be implanted following reports that the system — which circulates oxygenated blood when the patient's heart is failing — is associated with more deaths, strokes and device problems than a competing system made by Abbott Laboratories.
Medtronic has reported more than 100 patient complaints involving a delay or failure in restarting the devices' implantable blood pump, "which led to a total of 14 deaths and 13 pump removals," the FDA says. About 2,000 HVADs are currently implanted in the U.S., out of 4,000 implants worldwide.
"Medtronic initiated this action in light of a growing body of observational clinical comparisons indicating a higher frequency of neurological adverse events, including stroke, and mortality with the HVAD System," Medtronic said in its statement. "Considering these findings and the availability of alternative devices, Medtronic made the decision to stop the distribution and sale of the HVAD System."
The HVAD is intended for advanced-stage heart failure patients. Initially approved as a temporary "bridge" to full heart transplant, such devices are now allowed to be implanted as a "destination" therapy, with no intention of removing it.
Unlike implantable pacemakers and defibrillators, which restore a normal heart beat and cost several thousand to several tens of thousand dollars, a ventricular-assist device pumps a patient's blood for them and carries a six-figure price. A 2017 analysis found the mean cost of purchasing and implanting a ventricular assist device was $175,000.
Medtronic refers to its device as the Medtronic HVAD System, while the FDA calls it the HeartWare Ventricular Assist Device — named for its former manufacturer, HeartWare International, which Medtronic acquired in 2016.
The HeartWare system has been the subject of numerous serious recall actions over the years, including three Class I recalls this year, according to industry publication MedTech Dive.