"Medical Laboratory" by ben.dracup, CC BY 2.0.One FDA report says a heart monitor's AI rejected true pauses and flagged false fast rhythms
The FDA received a malfunction report for the Linq ii insertable cardiac monitor made by Medtronic singapore operations. According to the report, the device's AI algorithm rejected true pause episodes as false and detected false ventricular tachycardia episodes.
FDA MAUDE report 25093688
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