
Two deaths, 109 injuries in U.S. linked to faulty Philips heart monitor device
NL TimesAt least two deaths and over a hundred injuries have been linked to a malfunctioning heart monitoring device from Philips and its subsidiary, Braemer. When fully operational, the Mobile Cardiac Telemetry Monitoring is supposed to “process, analyze, display, and report symptomatic and asymptomatic cardiac events” from the electrocardiogram data it receives, according to the U.S. Food and Drug Administration. But the device with the model number BTPS-1000 sometimes failed to notify healthcare providers of serious cardiac events during the period from July 2022 to July 2024. In 2021, the healthcare technology company had to recall millions of home sleep apnea devices after discovering that the insulating foam could crumble and come loose if cleaned with certain agents.
History of this topic

Company that made millions of defective sleep apnea machines ordered to overhaul manufacturing
Associated Press
The number of claims for damages against Philips in the US is increasing
NL Times
Philips restructuring: Massive layoffs and recall of sleep apnea devices
NL Times
Philips to recall more sleep apnea masks after pacemaker problems emerge
Dutch News
Philips to recall more sleep apnea masks after pacemaker problems emerge
Dutch News
Philips expands respirator recall
NL Times
Philips investigating patient's death after ventilator failure
NL Times
Sleep apnea device issues a blow to Philips' profits
NL Times
Four Dutch users take Philips to court over sleep apnea device
Dutch News
Four Dutch users take Philips to court over sleep apnea device
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