The patient experienced an arrhythmia that met medical doctor notification (mdn) requirements that was not transmitted during the wear period.The investigation revealed a potential algorithm sensitivity issue with the device.The healthcare provider (hcp) was immediately notified, and irhythm learned that the hcp was already aware of the patient's arrhythmia and that no treatment would be provided at this time.There were no delays in treatment, and no adverse events, such as death or serious injury, are known to have occurred.
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