Physiomesh Hernia Mesh Withdrawal From Market
Ethicon, a subsidiary of Johnson & Johnson, recently withdrew the surgical mesh Physiomesh® from the market. The product is commonly used in hernia repair procedures. Patients who have large hernias or multiple hernia procedures may need to have surgical mesh put in place to prevent reemergence of the hernia. This flexible mesh is placed with a laparoscope and has been used since March 2010.
Complications from Physiomesh
Some patients who had Physiomesh involved in their procedure are developing complications as a result of the mesh.
Including, but not limited to:
- Infection
- Chronic pain
- Organ damage
- Migration of the mesh
- Mesh shrinkage
- A need for corrective surgery or revision
Removed from the Market
Ethicon voluntarily withdrew the product from the market in May of 2016 after multiple reports of severe complications and increased risk of side effects.
Do I have a case?
Elk & Elk attorneys are available to investigate claims involving Ethicon Physiomesh. If you had laparoscopic hernia surgery after March 2010 and have suffered from complications, you may be entitled to financial compensation. Call 1-800-ELK-OHIO for a free legal consultation, or contact us online.
