Two deaths, 109 injuries in U.S. linked to faulty Philips heart monitor device
2 months ago

Two deaths, 109 injuries in U.S. linked to faulty Philips heart monitor device

NL Times  

At 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
11 months, 2 weeks ago
The number of claims for damages against Philips in the US is increasing
1 year, 8 months ago
Philips restructuring: Massive layoffs and recall of sleep apnea devices
2 years, 1 month ago
Philips to recall more sleep apnea masks after pacemaker problems emerge
2 years, 6 months ago
Philips to recall more sleep apnea masks after pacemaker problems emerge
2 years, 6 months ago
Philips expands respirator recall
2 years, 6 months ago
Philips investigating patient's death after ventilator failure
2 years, 11 months ago
Sleep apnea device issues a blow to Philips' profits
3 years, 2 months ago
Four Dutch users take Philips to court over sleep apnea device
3 years, 4 months ago
Four Dutch users take Philips to court over sleep apnea device
3 years, 4 months ago

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