According to the FDA, more than one million hernia repairs are performed each year in the U.S. Hernia meshes are used by surgeons frequently. Usually, with various types of surgical treatments, the patient recovers. However, patients may be left with hernia mesh injuries due to complications from a defective mesh product.
The defective mesh products can cause a wide range of injuries such as organ damage, intestinal and bowel obstructions, adhesions, infections, and permanent nerve damage. They also cause other adverse side effects such as chronic pain, inflammation, hernia recurrence, and the need for additional or revision surgery to remove the mesh and rectify the problem.
If you have developed an illness or health complication as a result of using any hernia mesh medical device, you may be entitled to compensation.
Our attorneys at Keith Law provide dedicated, experienced legal representation to victims of hernia mesh injuries.
A hernia occurs when an organ, intestine, or fatty tissue squeezes through a hole or a weak spot in the surrounding muscle or connective tissue. They commonly occur in the abdomen.
According to the FDA, the most common types of hernias include:
Although surgery is the only treatment that can repair hernias, waiting and watching is an option for many people who don’t have complications or symptoms with an adult inguinal hernia.
In laparoscopic hernia repair, the surgeon makes several small incisions in the abdomen. Open repair involves a larger incision. Both laparoscopic and open repair can be performed with or without mesh.
Common symptoms of hernia mesh injuries are bloating, bulging, or bowel obstruction. The patient might feel heavy underneath their stomach. At times, they won’t be able to lift heavy things. They might feel exhausted even after doing nothing.
If you have a hernia mesh, some of the symptoms you can be on the lookout for are urinary issues, severe pain, irritable bowel, fever, fatigue, and constipation. These symptoms can occur within days or years after the mesh was installed. If you experience any of these symptoms, contact your physician immediately.
Numerous hernia mesh products have been recalled over the years. In 2005, C.R. Bard recalled various Kugel Mesh branded products after they were associated with numerous health complications like increased risk of bowel tears.
In 2012, Atrium was given a warning by the FDA for failing to recall its mesh products named C-QUR. In 2015, the company was instructed by a federal judge to stop manufacturing the subject product as a result of numerous complaints of infections from the public.
In 2016, Ethicon undertook a voluntary recall of its Physiomesh products after studies showed that its products were defective. The company was forced to issue notices to doctors and hospitals informing them to stop using the subject products as they increased the chances of hernia failure and other serious complications.
Hernia mesh medical devices have resulted in thousands of patients suffering from serious adverse health complications such as infections and organ damage.
Injuries related to this device can be avoided by using an alternative.
However, if you or your loved ones have suffered hernia mesh injuries in Arkansas, reach out to us so we can guide you through the best options available to you.