Hernia Mesh Recalled

Ethicon, of Johnson and Johnson, issued a voluntary recall of its Physiomesh™, Flexible Composite Mesh.

Hernias are most common in the abdomen, and may be caused by exertion, obesity or abdominal surgery. Hernia mesh was intended to repair hernias, occurring when an organ pushed through an opening in the muscle or tissue wall. Many people are suffering from major health problems from these devices. Physiomesh™ was recalled, as other brands like C-QUR™ mesh have been associated with similar problems.

Surgery Side Effect

Surgery is often needed to remove the mesh. Unfortunately, removal may not be possible.


The attorneys at Houssiere Durant Houssiere, LLP are experienced in handling medical device defect cases nationally; and are actively handling all hernia mesh cases. If you are experiencing problems after surgery with your hernia, mesh; or have already undergone a revision surgery, you may be entitled to compensation from the manufacturer. Call our experienced attorneys now at 888-881-8100 toll-free or fill our contact form for a free consultation.

hdhadminHernia Mesh Recalled