The patient experienced two arrhythmias that met medical doctor notification (mdn) requirements that was not communicated during the wear period.The investigation revealed that 1) a preliminary ecg interpretation provided to the physician was misclassified and 2) identified an additional arrhythmia that was not transmitted.Following the wear period and while compiling the final report, the interpretation was amended.The hcp was notified immediately, and irhythm learned that the hcp was already aware of the patient's arrhythmia and was treating it.No adverse events, such as death or serious injury, are known to have occurred.
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