Covidien Parietex Composite Mesh Lawsuit Claims Hernia Patch Dangerously Defective

|
Irvin Jackson

Add Your Comments

According to allegations raised in a hernia mesh lawsuit recently filed against Covidien and Medtronic, Inc., the Parietex Composite Mesh is defectively designed and a danger to patients, increasing the risk of painful complications following hernia repair. 

Following the failure of the Covidien Parietex mesh, resulting in the need for revision surgery, Louisiana filed a product liability complaint (PDF) against the medical device manufacturers on January 12, in the U.S. District Court for the Western District of Louisiana.

Lacassin indicates that she underwent surgery for hernia repair in November 2011, at which time doctors implanted the Covidien Parietex Composite Mesh.

Hernia Mesh Lawsuits

Did you or a loved one receive a hernia mesh?

Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery.

Learn More
SEE IF YOU QUALIFY FOR COMPENSATION
Is there a hernia mesh lawsuit? Find out if you qualify for a hernia mesh lawsuit settlement payout.
Is there a hernia mesh lawsuit? Find out if you qualify for a hernia mesh lawsuit settlement payout.

Hernia Mesh Lawsuits

Did you or a loved one receive a hernia mesh?

Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery.

Learn More
SEE IF YOU QUALIFY FOR COMPENSATION

“As a result of the implantation of the unreasonably dangerous and defective Parietex Composite Mesh, Plaintiff suffered injuries including, but not limited to, scarring, pain, recurrence, and additional surgery,” the lawsuit states.

The complaint indicates that numerous reports of problems with Parietex Composite Mesh have been submitted to the FDA, maintaining that Covidien and Medtronic misrepresented the safety and effectiveness of the hernia patch to the public and medical community.

“The absorbable collagen barrier on the visceral side of Parietex Composite Mesh fails to protect the body from the hydrophilic three-dimensional polyester textile on the parietal side because the absorbable collagen barrier breaks down after coming in contact with moisture and tears easily during handling. The composition of polyester is also weak and Parietex Composite Mesh is known to unravel causing the polyester fiber to detach and travel to other parts of the body inciting an inflammatory response,” Lacassin indicates in the lawsuit. “Parietex Composite Mesh further contracts over time causing tension to increase where secured by tacks and sutures resulting in tearing.”

Lacassin presents claims for construction or composition defect, design defect, inadequate warning, breach of warranty, negligence, and redhibition. The case joins a growing number of similar cases filed over design problems with different hernia mesh products sold in recent years. In addition to cases for Covidien Parietex Mesh, similar allegation have been raised in Ethicon Physiomesh lawsuits, Atrium C-Qur lawsuits, Bard Ventralex lawsuits and other claims.

Tags: Covidien, Hernia, Hernia Mesh, Parietex
Image Credit: |test caption

More Hernia Mesh Lawsuit Stories

1 Comments

fred
I have been suffering with inflammation, swelling and acute pain since the hernia operation. The operation took place March 23/2017. Have been back to see the surgeon 3 times since the operation. He said the pain could last for a year or may never resolve. At this point I have lost all confidence in this doctor as he had no empathy for my pain and suffering and how it impacted my life. . I need serious help; this problem is slowly killing me. Thank you for reading this Fred

Share Your Comments

This field is hidden when viewing the form
I authorize the above comments be posted on this page
Post Comment
Weekly Digest Opt-In

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

This field is for validation purposes and should be left unchanged.

MORE TOP STORIES

Link Between Hair Relaxers and Cancer To Be Examined by Court During Science Day
A federal judge has called for Science Day presentations to explain to the court the theories and evidence linking hair relaxer to increased cancer risks.
Lawyers Ordered to Engage in Talcum Powder Settlement Talks in MDL
A special mediator has been appointed to oversee negotiations between Johnson & Johnson and tens of thousands of women who say its talcum powder products caused them to develop reproductive system cancers.
Depo-Provera Wrongful Death Lawsuit Blames Injections for Fatal Brain Tumor
A wrongful death lawsuit claims a woman’s sister died of a Depo-Provera brain tumor which was not discovered until after her death.