The Food and Drug Administration announced that Philips recalled the software following 109 reported injuries and two ...
Some electrocardiogram events, such as atrial fibrillation or abnormally rapid heartbeats, over two years were not reviewed ...
The FDA is elevating a recall from Philips related to one of its wearable outpatient heart monitors, used to help detect ...
The FDA announced today that a Philips recall involving remote cardiac monitoring software is Class I, its most serious ...
Philips recalls software for mobile cardiac telemetry devices after patient injuries and deaths. Urgent medical device correction issued. Class I recall.
The Philips Hue Sync TV is a new subscription service that was announced, but is the entire model worth paying for? Read on ...
Medpage Today on MSN6d
Medicare for Renal Denervation; Cardiac Telemetry App Recall; Stroke Flags in EyesThe Centers for Medicare & Medicaid Services will review a potential national Medicare coverage policy for renal denervation ...
Philips sent customers a letter about the recall on Dec. 18, 2024, according to the FDA’s notice. The company has created a website called the “Prescriber Response Site,” where customers can review ...
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