As reported to coloplast, though not verified, the patient with this device experienced complications associated with transvaginal mesh products such as inter alia, dyspareunia, severe pelvic pain, urinary urgency problems, incontinence, and difficulty with daily activities.
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Additional information received on 02/08/2023 indicates that beginning 2/12/2018 the patient experienced trace blood and during intercourse, the husband felt something which resulted in a cut.Mesh visualized and palpated on anterior vaginal wall, extensive exposure of mid-urethral mesh.On 6/19/2020 vaginal exploration with complete removal of the altis sling.
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