The FDA is elevating a recall from Philips related to one of its wearable outpatient heart monitors, used to help detect ...

The Food and Drug Administration announced that Philips recalled the software following 109 reported injuries and two ...

The Centers for Medicare & Medicaid Services will review a potential national Medicare coverage policy for renal denervation ...

The FDA announced today that a Philips recall involving remote cardiac monitoring software is Class I, its most serious ...

Key Takeaways from the Cardiac Arrhythmia Monitoring Devices Market Report .On November 13, 2024, SmartCardia received FDA clearance for its Mobile Outpatient Cardiac Telemetry (OCT/MCT) system, which ...

the event recorder or loop monitor, and real-time mobile outpatient cardiac telemetry. Invasive rhythm evaluation options include the implanted loop recorder and cardiac electrophysiologic study ...

Philips recalls software for mobile cardiac telemetry devices after patient injuries and deaths. Urgent medical device correction issued. Class I recall.

Here are three recent recalls reported to the FDA: ...