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

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

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The common medical devices don’t work as well for Black patients. The FDA is now trying to do something about it.

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