Coloplast has not been provided any corroborating evidence to verify the information contained in this report.Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurrence.Should additional facts prompt us to alter or supplement any information or conclusions contained in the original mdr or in any prior supplemental reports, a follow-up report will be submitted.
|
As reported to coloplast, though not verified, legal representative stated the patient with this device experienced vaginal exposure of mid urethral device and postmenopausal bleeding.Patient had exam, diagnostic hysteroscopy, dilation and curettage, revision and repair of exposed mid urethral device under general anesthesia.Findings noted an endometrial polyp on the anterior vaginal wall.Approximately 4 cm of exposed graft material was dissected free and removed and submitted to pathology for identification.
|