During a literature search, atricure determined that a patient treated between 2015 and 2018 had an adverse event, which may have been caused by or contributed to by the emr2 device.The literature reported a perforation.Surgical intervention was necessary and the patient fully recovered.Atricure reviewed other complications listed within the paper, but were unable to find a cause or contribution to an atricure device.This adverse event is the result of a procedural complication.No device malfunction was reported.
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