Patients are currently filing lawsuits over allegations that hernia mesh manufacturers have created defective medical devices and have failed to warn patients and doctors of potential health complications adequately. These lawsuits are being filed against manufacturers such as Ethicon, C.R. Bard, and Atrium Medical Corp.
The claims from patients are complaints that the hernia mesh used for their hernia surgeries has caused health issues such as chronic pain, infection, adhesions, hernia recurrence, bowel perforation, bowel obstruction, mesh migration, mesh rejection, and more. Some patients are required to undergo hernia revision surgery.
Those who require hernia revision surgery or have experienced health complications similar to those listed above have the option of filing a defective medical device lawsuit against the manufacturer. Broughton Partners provides a legal case generation service that helps personal injury attorneys find injured patients who have received defective hernia mesh implants. We deliver pre-qualified leads with retained plaintiffs. The hernia mesh lawsuit leads your law firm will receive are qualified retainers and have been fully reviewed for lawsuit eligibility. If your law firm is looking to help more patients who have been injured due to harmful hernia mesh implants, call Broughton Partners today and start getting connected with hernia mesh lawsuit leads.