As reported to coloplast, though not verified, legal representative stated the patient with this device experienced vaginal device erosion, bleeding, discharge, odor, pelvic pain, urinary incontinence.Patient had the device revised, cystoscopy and debridement of infected wound bilaterally under general anesthesia.
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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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