Thousands of women in the United States and many other parts of the world are alleging transvaginal mesh devices used to correct pelvic organ prolapse (POP) and stress urinary incontinence (SUI) are causing serious complications and permanent injury. Class action has been filled in Australia and Canada against transvaginal mesh manufacturers.
These could potentially become the biggest class actions those countries have ever seen. Likewise, in the United States, transvaginal mesh litigation could become the largest case of product injury litigation ever.
A handful of medical device corporations, including Johnson & Johnson’s Ethicon Boston Scientific, C.R. Bard, American Medical Systems, Coloplast, and Mentor manufacture about 20 transvaginal mesh kits, which are designed to replace “native tissue repairs” and shore up prolapsed organs.
Unfortunately, none of these devices were adequately tested before they were approved for market, and only after they were implanted in hundreds of thousands of women did the frequency and severity of their complications come to light. Most of these complications involve erosion(also called mesh exposure ,extrusion, or protrusion) brought about by what physicians call “compliance mismatch” according to Australian uro gynecologist Richard Reid, who is treating the lead Plaintiff in Australia’s transvaginal mesh class action.
The fibrous polypropylene mesh acts like a cheese grater on the softer organs and tissues in contacts, This grating effect can rub a hole in the vaginal wall, or it may perforate the bladder or other organs or shred surrounding tissue, resulting in intense pain, neuro muscular problems, inability to walk, dyspareunia (painful sexual intercourse), vaginal scarring and shrinkage, bleeding, infection and severe emotional distress often to the point of suicidal thoughts. From 2008 to 2011, seven deaths were attributed to transvaginal mesh complications. Mesh complications may also arise when the device shifts out of place or breaks apart.
Tom Margolis, a Bay Area pelvic surgeon who specializes in removing transvaginal mesh, says that all transvaginal mesh kits are fundamentally flawed because they contradict the core principles of surgery. Dr. Margolis recently testifies at a U.S Food and Drug Administration meeting that passing a sterile, porous mesh device through the vagina for implantation violates the Golden Rule surgery. He stated: “You shall never implant a synthetic object in anyone’s body, anywhere, if it’s contaminated. To do so is to put the patient at serious risk of infection.”
The problems with transvaginal mesh exacerbated by the difficulty of removing the devices when things do go wrong. The thin fibrous mesh quickly becomes intertwined and incorporated with the surrounding tissue. Complete removal of mesh can be extremely difficult, if not impossible, requiring multiple surgeries over years. Mesh removal is also very dangerous because, as Dr. Margolis explained, it’s like trying to extract rebar from a hardened concrete slab without damaging the surrounding water mains and electrical cables.
The FDA issued its first transvaginal-mesh Public Health Notification in 2008 after detecting a pattern of adverse events in its post market surveillance of the devices. From 2008 to 2011, the agency received 2,874 adverse event reports involving transvaginal mesh devices- a fivefold increase in just three years. In 2011, the agency issued a stronger warning, saying that mesh failure rates could be as high as 10 percent, citing recent studies that found the devices may have ample risks without any apparent benefit. In 2012, the FDA ordered the manufacturers to test their devices for safety and efficacy. Any transvaginal mesh kits that failed could be removed from the market.
It was most unfortunate that the FDA allowed these potentially dangerous products onto the market in the first place. The growing mesh problem underscores flaws with the 510k approval process the FDA relies on to expedite many medical devices to market. This system puts medical devices on a fast track through the approval process if they are substantially similar to already approved devices. According to Drug watch, trans-vaginal mesh devices fast tracked through FDA approval were based on a device that was recalled from the market years later due to serious structural flaws and other problems. Ultimately, it is the manufacturer’s responsibility, however, to test its products for safety and effectiveness before they seek government approval for them. Litigation to hold manufacturers accountable is critical to the prevention of similar health disasters in the future.