The patient experienced an arrhythmia that met medical doctor notification (mdn) requirements that was not communicated during the wear period.The investigation revealed that a preliminary ecg interpretation provided to the physician was misclassified.Following the wear period and while compiling the final report, the interpretation was amended.The hcp was notified immediately, and irhythm learned that the patient¿s care team is considering the treatment options.No adverse events, such as death or serious injury, are known to have occurred.
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