As women across the country continue to suffer complications from the use of Johnson & Johnson’s transvaginal mesh devices, a new report reveals that the design of the bladder mesh was based on recalled transvaginal mesh devices that had been taken off the market more than ten years ago due to safety problems. The devices were designed to treat a condition called pelvic organ prolapse.
Transvaginal mesh, also referred to as a pelvic sling or bladder mesh – has been subject to increased scrutiny as the result of problems from its use including:
• Vaginal pain
• Injury to nearby organs
• Bladder perforations
• Vaginal mesh hardening
If you or someone you love has experienced complications from the use of transvaginal mesh, it is important to speak with an experienced defective medical device attorney who can provide critical advice concerning your injuries. In many circumstances, you may be entitled to monetary compensation.
Here, reports indicate that even though the FDA had pulled a similar mesh design created by Boston Scientific Corporation from the market, the FDA continued approving the similarly designed vaginal mesh created by Johnson & Johnson. Now, makers of the implant face more than 600 lawsuits nation wide from women who have suffered serious injuries from the devices. The devices were approved as part of FDA’s 510(k) process that allows “fast-track” approval of medical devices where a similar device is already on the market. The fast-track process allows new devices to be approved with little – if any – testing on patients.