Medical products are intended to make our lives better, to address illnesses and physical conditions, and to help medical professionals render the best medical care that they can provide. And while many medical devices are successful in helping to facilitate these goals, there are a number of devices that end up doing more harm than good. In some cases, the harm results from a manufacturer’s failure to design the device in a reasonably safe manner. In some cases, the harm is a result of a company’s negligence. In others, the harm results from a company’s desire to prioritize profits over patients’ health and safety.
One of the most discussed dangerous medical products in recent news is pelvic mesh. There are a variety of manufacturers that have developed pelvic mesh products. In general, the device is intended to support damaged or weak tissue. They’ve also been used to address stress urinary incontinence in women. The device is also often known as vaginal mesh or surgical mesh.
Recently, a jury in Pennsylvania awarded a plaintiff a $20 million verdict in a lawsuit against Johnson & Johnson involving one of its pelvic mesh products. The plaintiff alleged that she received the company’s product during a surgical procedure to address her stress urinary incontinence. After one month, the woman reported experiencing severe discomfort and pain. It was later determined that the mesh product began to erode. Her treating physicians performed a number of surgeries to repair the damage, but they were ultimately unable to remove all of the mesh shards.