Hernia Mesh Leads
Reach patients who suffered mesh migration, chronic pain, infection, or bowel obstruction after hernia repair surgery using defective surgical mesh products.
Hernia Mesh Litigation
Surgical mesh used in hernia repair procedures has been linked to a high rate of serious complications including mesh migration, infection, adhesion to organs, and chronic pain. Manufacturers including Atrium, Bard, Ethicon (Johnson & Johnson), and Covidien have faced thousands of lawsuits alleging their mesh products were defectively designed and inadequately tested. Many patients require additional surgeries to remove or revise the failed mesh implants.
Associated Conditions
- Mesh migration and displacement
- Chronic pain at the surgical site
- Infection and abscess formation
- Bowel obstruction or perforation
- Mesh adhesion to internal organs
- Hernia recurrence
- Need for revision or removal surgery
Claimant Eligibility
- Underwent hernia repair surgery with implanted surgical mesh
- Experienced complications such as pain, infection, or mesh failure
- Required revision surgery or mesh removal
- Mesh implanted by a qualifying manufacturer (Atrium, Bard, Ethicon, Covidien, or others)
- Complications arose within ten years of the original mesh implantation
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