Note: this report pertains to second of two devices used during the same procedure.Refer to manufacturer report: 3005099803-2018-01939 for the first associated device information.It was reported to boston scientific corporation that two capio¿ slim devices were used during a sacrospinous ligament fixation procedure.According to the complainant, during the procedure, during deployment of the first device [3005099803-2018-01939] through the sacrospinous ligament then into the capio cage, the suture broke and the dart was found in the capio cage.A second device [mfr.Report #: 3005099803-2018-01940] was opened and the same issue occurred.The dart of the second device was also found in the capio cage.The procedure was completed with a third capio slim device.There were no patient complications reported as a result of this event.The patient's condition at the conclusion of the procedure was reported to be normal and stable.
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