The most common injuries associated with recalled hernia patches are pain, infection, hernia recurrence, adhesion (scar-tissue), and organ damage, according to the FDA.
Need a Texas Hernia Patch Recall Lawyer? Collen A. Clark is a true advocate for his clients and is passionate about helping Texans that have been injured or wronged. If you or a loved one was injured by a recalled mesh patch or plug, you should contact our lawyers immediately. You may be entitled to compensation by filing a lawsuit.
FDA Warning: Hernia Mesh Patch Complications
Recalled hernia mesh patches were the main cause of bowel perforation and obstruction complications, according to a Safety Warning issued by the FDA. Thousands of lawsuits have been filed by people who were injured by complications of recalled products.
Hernia Mesh Patch Recalls
Ethicon Physiomesh Hernia Patch Recall
In May 2016, Ethicon Inc. recalled Physiomesh Composite Flexible Mesh in several countries in Europe, Australia, and other parts of the world after a large study found higher rates of hernia recurrence and re-operation.
Physiomesh was not recalled in the United States — it was withdrawn from the market without any warnings by the FDA. Ethicon is facing a growing number of lawsuits in the U.S. from people who experienced:
- Hernia recurrence
- Dense adhesions
- Bowel obstruction
- Chronic pain
Atrium C-QUR Hernia Patch Recall
In June 2013, Atrium Medical Corp. recalled the C-QUR patch because the Omega-3 (fish oil) coating could peel off and stick to the inside of the package when exposed to high humidity and moisture inside the package.
The recalled C-QUR Patch was never actually removed from the market — only the packaging was recalled. However, lawsuits have been filed by people who say the fish oil coating peeled off in their body and caused the following side effects:
- Allergic reactions
- Adhesions (scar-tissue)
- Body rejects mesh
- Mesh migration
Kugel Hernia Patch Recalls
C.R. Bard/Davol issued three Class I recalls for the Kugel Composix Hernia Patch between 2005 and 2007. The recalls were issued because a plastic ring that helped “spring” open the mesh could break.
Around 3,000 lawsuits were filed by people who suffered organ damage, bowel perforations, and/or chronic intestinal fistulae (abnormal connection between the intestines and other organs). These lawsuits were resolved with a $184 million settlement in 2011.
Counterfeit Hernia Patch Recalls
In June 2010, the FDA issued a Class I recall for counterfeit hernia patches that were falsely labeled as C.R. Bard/Davol Flat Mesh (commonly known as Marlex Mesh). The counterfeit products are not sterile, although they are labeled sterile. The edges are not sealed, which could allow the mesh to unravel.
List of Gore Hernia Patch Products
The following is a list of hernia patch products that are sold by Gore Medical:
- Gore-Tex Soft Tissue Patch
- Gore Bio-A Hernia Plug
- Gore Dualmesh Biomaterial
- Gore Dualmesh Plus Material
- Gore Synecor Intraperitoneal Biomaterial
- Gore Synecor Preperitoneal Biomaterial
Need a Hernia Patch Recall Lawyer in Texas?
Collen A. Clark is a true advocate for his clients and is passionate about helping Texans that have been injured or wronged.
Collen’s amazing success in the courtroom and well known dedication to his clients has earned him the recognition of his peers as one of The Top Trial Lawyers in Texas.”
The Clark Firm has assembled a team of trial lawyers with more than 100 years experience, participation in over 600 jury trials and $260 million in verdicts and/or settlements. Please use the form below to contact our Texas hernia mesh lawyers for a free lawsuit review.