Composix Kugel Mesh Patch Litigation at The Lanier Law Firm
Originally developed by Dr. Robert D. Kugel, the Composix Kugel Mesh Patch was designed to repair ventral (incisional) hernias caused by the thinning or stretching of scar tissue that forms after surgery.
However, in December 2005, several lots of the Composix Kugel Mesh Patch were recalled. In January 2007, Davol Inc., the manufacturer of the mesh patch, updated the recall to include additional lots. Between 2002 and the time of the recall, approximately 32,000 affected units - now subject to the recall - were sold worldwide.
The Composix Kugel Mesh Patch is placed behind the hernia and held open by a "memory recoil ring." This ring allows the patch to be folded for insertion and, once in place, spring open and lay flat. It was this memory recoil ring that caused the Composix Kugel Mesh Patch patch to be recalled.
In many cases, the memory recoil ring can break while being inserted. This can lead to bowel perforations or rupture and chronic intestinal fistulae (abnormal connections or passageways between the intestines and other organs).
Patients could experience symptoms such as unexplained or persistent abdominal pain, fever, or tenderness at the implant site, and may require additional surgeries to repair damage and remove the mesh patch.
If you or a loved one has used the Composix Kugel Mesh Patch and suffered side effects, please contact our office for a free evaluation.
Composix Kugel Mesh Patch Information Links:
FDA Composix Kugel Mesh Patch Recall Notice
Davol Internet Homepage Expanded Composix Kugel Mesh Patch Recall Notice
