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The FDA granted Zoll Medical premarket approval for its full portfolio of external defibrillators, including the AED Pro and AED Plus automated external defibrillators and the R Series and X Series monitor defibrillators. Among the devices' featur...
Posted: January 17, 2018, 5:44 pm
Asahi Kasei (TYO:3407) subsidiary Zoll Medical and the FDA are warning about an error code displayed by a model of its LifeVest wearable automatic external defibrillator that was involved in a patient’s death. Patients using LifeVest 4000 models w...
Posted: January 17, 2018, 8:21 am
CHELMSFORD, Mass. — ZOLL ® Medical Corporation, an Asahi Kasei Group Company that manufactures medical devices and related software solutions, today announced that the 2018 ZOLL PULSE Awards is now open for nominations. Nominations can be submitte...
Posted: January 17, 2018, 7:16 am
A patient who died when a Zoll LifeVest failed to work has led the manufacturer Zoll Medical and the FDA to issue a safety alert for physicians and patients using the wearable heart monitor and external defibrillator. The device failure was traced...
Posted: January 17, 2018, 4:58 am
The Zoll LifeVest 4000 is a wearable defibrillator used to treat life-threatening abnormal heartbeats (arrhythmias) in adults and children who are at risk for sudden cardiac arrest and are not candidates for, or refuse, an implantable defibrillator.
Posted: January 17, 2018, 12:00 am

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