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 ...
Philips recalls software for mobile cardiac telemetry devices after patient injuries and deaths. Urgent medical device correction issued. Class I recall.
The 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 ...
CNN’s Alex Marquardt sent a message to a colleague: “We gonna nail this Zachary Young mf---er.” There were no dashes in the ...
to immediately cease the sale of certain products manufactured by affiliates of Philips Lighting brand, and also ordered the recall and destruction of infringing products distributed in the market ...