The US Food and Drug Administration is alerting physicians about a heart pump recall initiated late last year: Medtronic issued a recall for its HeartWare ventricular assist device (VAD) pump implant ...

The US Food and Drug Administration is alerting physicians to another Class I recall for the HeartWare ventricular assist device (HVAD), this time related to controller port damage. The FDA alert, ...

Medtronic is recalling the pump implant kit for its HeartWare Ventricular Assist Device (HVAD) because the device may fail to initially start, restart, or have a delay in restarting after the pump ...

Medtronic’s decision to stop selling its HeartWare ventricular assist device comes after a spate of Class I recalls for the blood pump linked to about a dozen deaths and more than 100 complaints.

After a pair of others that began in April and May, Medtronic began alerting customers to its latest safety event for the HeartWare Ventricular Assist Device at the end of June. (Photo by Sarah ...

HHS unveiled a new Alzheimer's and dementia plan in Fort Lauderdale focused on prevention and early detection. Here is what is promised and proven. Final CDC Data Put U.S. Fertility Rate at Record Low ...

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Please provide your email address to receive an email when new articles are posted on . The FDA has designated Medtronic’s recall of its ventricular assist device batteries due to electrical faults ...

SALT LAKE CITY- Surgeons at University of Utah Hospital have performed the hospital’s first implant of a new generation left ventricular assist device (LVAD) using the HeartWare HVAD. The tiny, ...