The U.S. Food and Drug Administration issued its most serious type of recall for 348,616 Medtronic defibrillators, saying they are at risk for delivering "a reduced-energy shock or no shock at all," ...

The recalled devices pose a risk of reducing energy shock, or giving no shock at all and may fail to correct a life-threatening arrhythmia, which can lead to cardiac arrest, other serious injury, or ...

Medtronic recalled 348,616 implantable cardioverter defibrillators and cardiac resynchronization therapy defibrillators because they might fail to deliver energy when high voltage therapy is needed, ...

Medtronic is recalling nearly 350,000 implantable cardiac devices due to continued problems with the delivery of high-voltage energy, according to an announcement from the US Food and Drug ...

MINNEAPOLIS -- Medtronic has issued a recall for over 348,000 defibrillators because there is a risk they deliver low shock, or no shock at all. The Class I recall - the most serious type of recall ...