The patient's attorney alleged a deficiency against the device.It was reported by the patient¿s attorney that as a result of having the product implanted, the patient has experienced hemorrhoids, constipation, urinary tract infection, cystitis (inflammation), urinary incontinence, blood, nitrates, many bacteria, leukocytes, white blood cells, red blood cells in urine (hematuria and bacterial infection), abdominal pain, anemia, low red blood cells, hemoglobin and hematocrit, high eosinophils, escherichia coli in urine, rectal bleed secondary to internal hemorrhoids (blood loss), dizziness, difficulty with bowel movement, blood while straining, weakness, constipation and moderate fecal retention, tiny calculus mid pole of the left kidney, lower pole of right kidney, small left renal cyst, low potassium (electrolyte imbalance), retention, enterocele, colovesical fistula, recurrence, pain, unspecified urinary problems, unspecified neuromuscular problems, organ perforation, pelvic pain, erosion, vaginal bleeding, unspecified bowel problems, unspecified perforation, recurrence, pelvic organ prolapse, stress migration and extrusion, cystocele, foreign body in patient, urethra disorder, female genital prolapse, additional surgical and nonsurgical intervention.
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