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Defective hernia mesh products have injured thousands of patients in recent years, leading to long-term health issues and subsequent personal injury lawsuits. Patients implanted with Surgipro mesh products have reported injury and should contact an attorney.
Recipients of hernia mesh implants that have experienced chronic pain, recurrent hernias, mesh migration, adhesions, fistula, bowel blockage and bowel perforation should contact a hernia mesh defect lawyer to discuss your legal options.
Medical Device companies like Covidien, Aspide, Atrium, Ethicon, Gore and Bard have all been named defendants in product liability lawsuits for marketing and distributing allegedly faulty hernia mesh implants.
If you have suffered from a Covidien Surgipro mesh injury dating back to 2005 to the present, you may have a viable case and could recover compensation through litigation.
Joe Lyon is a highly-rated Cincinnati, Ohio Medical Device Recall Attorney and Hernia Mesh Defect Lawyer investigating Covidien Surgipro injury cases for plaintiffs nationwide.
Covidien Surgipro Mesh Injury & Complications
Thousands of hernia mesh implant patients have reported injuries and complications to their doctor and the FDA adverse event database. Potential hernia mesh injuries may include:
- Chronic Pain
- Fistula
- Bowel Blockage
- Bowel Perforation
- Mesh Migration
- Adhesions
- Severe Inflammatory Response
- Recurrent Hernia
Defective Hernia Mesh Implants
Large medical companies have sold millions of mesh products, and many have helped patients return to a better quality of life. However, when their products are defective, those affected can contact a hernia mesh attorney and file product liability lawsuits and seek a settlement for their injuries, pain and suffering and long-term disability. Companies that have reportedly produced recalled hernia mesh devices include:
- Bard
- Aspide
- Atrium
- Ethicon
- Gore
- Covidien
Surgipro Hernia Mesh Settlement
The Lyon Firm is dedicated to representing injured hernia mesh implant patients when product defects are found to be the cause of an injury. We have the resources to engage large medical device companies and work with industry experts to build the strongest case possible.
If you have suffered a Surgipro mesh injury from 2005 until the present, including chronic pain, bowel blockage, organ perforation, bleeding, mesh migration, or revision surgery, contact The Lyon Firm to weigh your legal options.
