As reported to coloplast, though not verified, legal representative stated the patient with this device experienced recurrent stress urinary incontinence, vaginal device erosion, and midline exposure.The device was explanted under general endotracheal anesthesia and a retropubic top-down midurethral device from another manufacturer was implanted.
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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.
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