The device was originally prescribed to monitor arrhythmia associated with the symptom of syncope and collapse.The patient was hospitalized during the prescribed wear period.Specific information regarding when and for what reason the patient was admitted is not available.The device was returned and a final report was generated.When compiling the final report, a delayed mdn (md notification) for the first documentation of atrial fibrillation occurred on 5/19/2022, prior to the information regarding the hospitalization.This mdr submission represents an incident where the patient was hospitalized.The investigation revealed the device did not malfunction, it is unknown whether the use error caused or contributed to the hospitalization.This mdr is being filed out of an abundance of caution.
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