The Kugel Mesh Hernia Patch was designed to repair ventral hernias that are caused by thinning and stretching of the scar tissue which develops after a patient has undergone surgery. The Patch was approved by the FDA in November of 1996, and put on the market shortly after by Davol.

To speak with an experienced lawyer about your Kugel Mesh Hernia patch case, call (877) 701-0222 or contact us online.

Recalled in 2005 & 2006

In 2002, a larger patch was introduced to the market but was discontinued in 2005 due to numerous consumer complaints. It wasn’t until December 2005 that a voluntary recall was issued by the manufacturer. The recall was then expanded on March 2006 to include two other versions of the patch.

Some of the conditions experienced by patients from the use of the defective Kugel Mesh hernia patch are:

• Bowel obstruction; this is a partial or even total blockage inside the intestines resulting serious injury and pain
• Bowel perforation; an opening that forms inside the intestinal wall; these perforations are extremely dangerous and if left untreated can cause sepsis or even fatal blood infections
• Enteric fistulas; an abnormal connection is formed between two parts of the intestines which may result in extreme abdominal pain and infection that can spread into the bloodstream.

Although Davol knew of defects in the Kugel Mesh hernia patch, the early signs were ignored. If you have been injured by the use of this product we believe you should be compensated for the pain suffered. Call us (877) 701-0222 or contact us online to discuss your case and legal options. Your consultation is free.