Ethicon’s Physiomesh Withdrawal


In June of 2016 manufacturer, Ethicon, subsidiary of giant Johnson & Johnson, began to withdraw from the market the surgical mesh for hernias called Physiomesh. The product is a flexible composite mesh and it was found that revisions were needed in a large number of hernia repairs using Physiomesh. This market withdrawal was helpful in keeping the product from being used with patients in surgeries after the withdrawal, but was of no good for those already having surgery with Physiomesh and suffering consequences. In fact, it has been estimated that as of November, 2016 300,000 Physiomesh implants might have been placed after its approval by the U.S. Food and Drug Administration in 2010!

Complications from Physiomesh have been alleged as infection within and also around the mesh once it’s implanted. This can cause abdominal abscesses, intestinal fistula, bowel obstruction, and possible other complications. Complications have required major surgery in patients, while not correcting the original pre-surgical diagnosis. There have been at least 650 Adverse Event Reports to the FDA with no real consequences to Ethicon. It is expected that this will result in a very large number of lawsuits and a motion for Multidistrict Litigation (MDL) to consolidate all of the cases and fight the giant Ethicon.

If you or a loved one has been injured by Physiomesh, or any medical device, drug, or other product, consult your medical provider and please contact Inserra Kelley Sewell, Personal Injury Attorneys, to discuss your potential justice and entitlement to compensation for your damages.