Related manufacturer reference number: 1627487-2019-13192; related manufacturer reference number: 1627487-2019-13194.It was reported that patient had pain at the implantable pulse generator (ipg) site due to an unknown reason.The device system was explanted as a result to resolve the issue.During the explant procedure, the physician noted one of the leads had completely pulled out of the ipg header, however it is unknown which lead was pulled out of the header port.Leads were explanted as a result to resolve the issue.No further information is available at this time.
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