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 healthcare provider (hcp) was immediately notified, but it was unclear whether the patient would receive treatment.Despite several attempts to gather more information, no additional details were obtained.No adverse events, such as death or serious injury, are known to have occurred.
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