Most of the cases allege injury due to a defect in the patch, which surgeons implant at the site of a hernia. The patches consist of two layers of synthetic mesh bound by a flexible plastic “memory-recoil” ring. These rings are known to break at their welded joints after they have been surgically implanted, causing patients extreme abdominal pain, fever, soreness at the surgical site, bleeding, infection, fever, a range of other symptoms, and occasionally death.

Next month’s trial involves a case filed by plaintiff John Whitfield, who was allegedly injured by the surgical implantation of a defective Mesh Patch.

Bellwether trials have become increasingly common in mass tort litigation to help facilitate the federal court system’s caseload. In a bellwether trial, a plaintiff or group of plaintiffs are chosen by the United States Judicial panel on Multidistrict Litigation to represent all cases based on their similarities. The results are then extrapolated to the remaining cases, which helps reduce redundancy while indicating and gauging common trends.

The other three hernia patch lawsuits chosen for bellwether trial also involve allegations representative of a larger body of cases.

Davol, Inc., and the FDA issued three separate recalls of Kugel patches between 2005 and 2007. The majority of lawsuits have been filed by plaintiffs who received severe injuries when the defective patches broke after being surgically implanted, thus requiring additional surgery for their removal.

SOURCE: Hernia Patch Recall › hernia patch trial scheduled for march in federal MDL

If all goes well, the patient may consider his hernia fixed and go about living life normally. For many patients, however, the medical miracle goes awry. The plastic “memory recoil ring” sometimes fractures, causing bowel perforations or abnormal connections between the intestines and other organs known as fistulae. The damage not only causes severe pain, it can also lead to additional medical complications and death.

While the Kugel Mesh Patches have been recalled, doctors are finding other problems arising from medical mesh devices and implants. Boston Scientific manufactures aortic and carotid stents with mesh, but the surgical insertion tip sometimes detaches during surgery. The FDA requested a recall of the company’s defective stents and stent delivery system.

Mesh is also a component in a couple products that are used in the treatment of stress urinary incontinence (SUI) in women. Specifically, Mentor Corporation’s ObTape may disintegrate inside the body and lead to a multitude of adverse events.

The FDA advises patients to seek immediate medical attention if they experience symptoms that could be associated with any of the recalled hernia patch devices. Ring breakage can cause inexplicable and / or persistent abdominal pain, fever, tenderness at the implant site and any other unusual symptoms.

SOURCE: Hernia Patch Recall › Hernia patch and other mesh implants pose problems