THE INVESTIGATION IS STILL IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETE A SUPPLEMENTAL REPORT WILL BE FILED. UDI FORMAT UPDATED WITH AVAILABLE PRODUCT INFORMATION PER GUDID. H11: SECTION A THROUGH F - THE INFORMATION PROVIDED BY BD REPRESENTS ALL THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT / REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO BD.
D
Patient 0
IT WAS REPORTED BY THE PATIENT'S ATTORNEY THAT AS A RESULT OF HAVING THE PRODUCT IMPLANTED, THE PATIENT HAS EXPERIENCED VAGINAL MESH EXPOSURE, MESH EROSION, VAGINAL PAIN, DISCOMFORT AND TISSUE DAMAGE. SYMPTOMATIC PELVIC ORGAN PROLAPSES WITH SECOND-DEGREE UTERINE PROLAPSE, ANTERIOR VAGINAL DEFECT, PARAVAGINAL DEFECT, POSTERIOR VAGINAL DEFECT, AND PERONEAL DEFECT.