Related manufacturer reference numbers: 3006705815-2021-00638, 3006705815-2021-00639, 1627487-2021-01301.It was reported that the patient experienced ineffective stimulation.Imaging revealed one of the leads had migrated.In turn, surgical intervention was undertaken wherein all leads and anchors were explanted and replaced.During the procedure, it was discovered that one of the anchors was broken.Post-operatively, stimulation therapy was restored.It is unknown which lead migrated and which anchor was broken, therefore all applicable devices are being reported.
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