“…In most facilities, therefore, surgeons created a mesh insert by cutting polypropylene mesh (Gynemesh PS; Ethicon, Somerville, NJ, USA or Polyform synthetic mesh; Boston Scientific, Natick, MA, USA) to match the pattern of the Prolift System (Ethicon, Somerville, NJ, USA), other kits, or the original pattern. 7,8 TVM surgery reportedly involved the risk of complications during or after surgery, such as injury of the bladder, rectum, and ureter, accidental massive bleeding/hematoma, urinary dysfunction, infection, dyspareunia, chronic pain, mesh erosion/exposure, and vaginal scarring. [9][10][11][12][13] In 2019, The US Food and Drug Administration ordered the manufacturers of all surgical mesh products indicated for the transvaginal repair of POP to stop selling and distributing their products.…”