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 ...
Doctors have long lamented being forced to use devices on pediatric patients off-label, putting them at greater risk of a medical malpractice lawsuit in the event that something goes wrong. The FDA ...
Zoll Medical Corporation, which received FDA clearance a few years ago for both home and hospital versions of its wearable defibrillator LifeVest, is now dealing with a range of lawsuits and FDA ...
The Health Products Regulatory Authority (HPRA) has issued a safety notice affecting a Zoll Powerheart defibrillator model which warns that the device may not deliver therapy when needed. The notice ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback