If you have been completely in the dark about the work about defective hernia repair products out there, then this is your chance to get caught up. We have an excellent blog about recent happenings to keep you informed. But, lets talk about the largest developments. In April of 2010, the FDA urged patients to determine if they have a Bard Composix Kugel Patch. The U.S. Food and Drug Administration recently issued a “Class 1” recall of these hernia repair patches because the defect associated with the use or exposure to the Kugel Hernia Patch has a reasonable probability to cause serious adverse health consequences, including death, according to the FDA. Patients can view a complete list of the patches in the recall by contacting us here and we will determine if you or your loved one had received one of these problematic patches. If you would like to lean more about recalls, be sure to head over to our page with more information.