The sample was not returned.The finished product met all specifications prior to potential complications associated with the proper implantation of the pelvilace¿ to system may include, but are not limited to: postoperative hematoma, which may occur following the implant procedure.Temporary urinary retention, bladder outlet obstruction, and voiding difficulties associated with over-correction/too much tension placed on the implant perforations or lacerations of vessels, nerves, bladder or bowel, which may occur during needle passage transitory irritation at the operative wound site, which may elicit a foreign body response that leads to inflammation, infection, or erosion at the implant site being released for general distribution.The instructions for use which accompanies all devices currently addresses potential risks associated with surgically implanted materials.The instructions for use states in the adverse events: ¿ (b)(4).
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The patient's attorney alleged a deficiency against the device.Per additional information received, the patient has experienced abdominal pressure, stress incontinence, urge incontinence, nocturia, post-hysterectomy vaginal vault prolapse, omental adhesions, and a cystocele.She has required one surgical intervention.
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