Philips Issues Class I Recall of Cardiac Monitoring Software After Two Deaths
Philips has initiated a Class I recall of its remote cardiac monitoring software following reports of 109 injuries and two deaths, according to the U.S. Food and Drug Administration (FDA). The recall is linked to the company’s Monitoring Service Application (MSA), which processes electrocardiogram (EKG) data from mobile cardiac outpatient telemetry devices. This development highlights […]
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