Lawyers In Physiomesh Lawsuit Consolidation To Present Oral Arguments Next Week

   

Physiomesh Lawsuit Filings Allege Failure Of Hernia Mesh Causes Infection, Hernia Recurrence, Severe Pain, And Other Injuries.

hernia-mesh lawsuits-physiomesh-lawsuit-physiomesh-failures-recall-complications-problems-lawyerPhysiomesh Lawsuit News: A year after Ethicon Inc. voluntarily withdrew its Physiomesh hernia mesh from the world market, a federal judicial panel will hear oral arguments on consolidating all federally filed Physiomesh lawsuit. The hernia mesh lawsuits allege Ethicon’s Physiomesh Flexible Composite mesh is defective and causes plaintiffs to suffer abdominal pain, bowel obstruction, infection, fistulas, hernia recurrence and other injuries. The U.S. Judicial Panel on Multidistrict Litigation has scheduled a hearing on May 25 at the John H. Wood, Jr. Courthouse in San Antonio, Texas.

Southern Med Law’s attorneys currently represent clients in physiomesh lawsuits. The firm has substantial knowledge on medical and legal issues involved in Physiomesh lawsuits filed against Johnson & Johnson’s subsidiary, Ethicon Inc. (Physiomesh lawsuit Case No. 4:17-cv-00188, U.S. District Court, Eastern District of Texas)

“Plaintiffs in these physiomesh lawsuits not only allege suffering permanent bodily injuries from Physiomesh, but also claim to have suffered mental and physical pain and economic losses,” says Dr. François Blaudeau, founder of Southern Med Law, who is an attorney and highly regarded practicing physician.

If you believe you have suffered serious hernia mesh injuries from Physiomesh Flexible Composite Mesh, you may be entitled to compensation from Ethicon. To speak with one of the firm’s attorneys regarding a no-obligation legal review on cases involving Physiomesh hernia mesh failure, you can call 1-205-547-5525 or visit www.southernmedlaw.com for further information or to fill out an online contact form.

In March, several plaintiffs involved in Physiomesh lawsuits filed a motion asking the JPML to transfer 18 hernia mesh complaints to the Middle District of Florida for coordinated pretrial proceedings. The plaintiffs said the Physiomesh complaints have common allegations and they expect filings of “hundreds of additional cases” in the near future. In Ethicon’s response to the plaintiffs transfer motion, the company said consolidation is not appropriate because there are more individual issues involved than common issues. A total of 37 Physiomesh lawsuits had been filed by the time Ethicon responded to the plaintiffs’ request in April. (In Re: Ethicon Physiomesh Lawsuits – MDL-17-22 Hernia Mesh Products Liability Litigation)

Ethicon’s Physiomesh Flexible Composite Mesh received 510(k) clearance from the U.S. Food and Drug Administration (FDA) in 2010. The large pore, multi-layered device is used in minimally invasive ventral hernia repair. Ethicon voluntarily withdrew Physiomesh after reviewing unpublished data from two large European hernia registries. The data showed Physiomesh had higher rates of revision surgeries and hernia recurrence after a minimally invasive ventral hernia repair compared to other meshes. Since Ethicon could not instruct surgeons on what might lead to a reduction in the recurrence rate, the company said it would withdraw the device from the world market.
[https://www.swissmedic.ch/recalllists_dl/13779/Vk_20160525_11_e1.pdf]

The first trial for a Physiomesh lawsuit has been scheduled for January 22, 2018 in the District of Southern Illinois, according to court records. The lawsuit involves an Illinois man who was implanted with the Physiomesh Flexible Composite Mesh in 2013. Two years later, the man was hospitalized due to an infection around the mesh which caused two abdominal abscesses and an intestinal fistula, the complaint said. The man underwent surgery to debride the abscesses. The Physiomesh complaint alleges the hernia mesh was defective d unreasonably dangerous and Ethicon failed to warn the medical community about the risks associated with its device. (Physiomesh Lawsuit Case No. 3:16-cv-00368, U.S. District Court, Southern District of Illinois)

About Southern Med Law And Filing A Physiomesh Lawsuit

Throughout his career, Dr. Blaudeau has worked hard to develop a strong reputation in healthcare litigation. His first-hand knowledge of medicine has made the Southern Med Law team an aggressive and effective advocate for those who were harmed due to negligent medical device manufacturers. If you or someone you care about were harmed by Physiomesh Flexible Composite Mesh, please contact Southern Med Law today to learn more about your legal rights. Call today for a free, no obligation hernia mesh lawsuit review by filling out our online form, or by calling the office directly at 205-547-5525.

Contact:
Southern Med Law
François M. Blaudeau, MD JD FACHE FCLM Esquire
2224 1st Avenue North
Birmingham, Alabama 35203
Phone: 205-547-5525
Fax: 205-547-5526
francois@southernmedlaw.com
www.southernmedlaw.com

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