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PERMACOL MESH


Medical Device Injury Lawyer investigates defective hernia mesh products for injured plaintiffs nationwide
Nationwide Success

Permacol Hernia Mesh Lawsuits

investigating mesh device injury & complications

Hernia mesh implant recipients who have suffered from chronic pain, infection, revision surgery, fistula, adhesions, bowel perforation, bowel blockage or other related injuries should seek medical attention and contact a hernia mesh recall attorney to determine your legal options in recovering medical costs and damages related to Permacol mesh injury.

The Lyon Firm has experience holding medical device companies like Covidien, Bard, Atrium, Aspide and Ethicon liable for injuries caused by hernia mesh products. Covidien’s Permacol mesh implant has allegedly caused hundreds of injuries related to complications with the mesh device.

Joe Lyon is a highly-rated Cincinnati, Ohio product liability lawyer and medical device recall attorney reviewing Permacol mesh injury cases for injured plaintiffs.

Covidien Hernia Mesh

The following products are being investigated for potential design defects and related injury caused by the mesh devices:

  • Permacol
  • Surgipro
  • Parietex
  • Parietene

Permacol Mesh Injury Lawsuits

Covidien has a had a history of mesh product recalls after manufacturing recalled medical devices. The devices have allegedly injured an unknown number of patients and litigation continues. Common Permacol mesh injury may include:

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ABOUT THE LYON FIRM

Joseph Lyon has 17 years of experience representing individuals in complex litigation matters. He has represented individuals in every state against many of the largest companies in the world.

The Firm focuses on single-event civil cases and class actions involving corporate neglect & fraud, toxic exposure, product defects & recalls, medical malpractice, and invasion of privacy.

NO COST UNLESS WE WIN

The Firm offers contingency fees, advancing all costs of the litigation, and accepting the full financial risk, allowing our clients full access to the legal system while reducing the financial stress while they focus on their healthcare and financial needs.

photo of attorney Joe Lyon reviewing permacol mesh
A Voice for Those who have suffered

Why are these cases important?

Defective medical device litigation helps to improve patient safety and holds medical device companies accountable when defective products injure plaintiffs and clients.

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Questions about Hernia Mesh Litigation

Can I file a hernia mesh lawsuit?

Attorneys claim several hernia mesh devices were not properly tested before they were marketed and distributed as safe medical instruments.

The companies currently face thousands of pending hernia mesh injury lawsuits. If you have had surgery to treat a hernia using a device and you experience any signs or symptoms of recurrence of the hernia, please consult with a medical and legal expert. The Lyon Firm has experience litigating cases against medical device manufacturers.

Attorneys contend that some hernia mesh devices are not properly tested before they are distributed to the public as safe products. Device companies like Gore, Aspide, Ethicon, Bard, Covidien and Atrium have settled hundreds of lawsuits and currently face countless more injury claims.

If you are unsure about the mesh manufacturer and product used in your surgery and have questions about your hernia repair, contact your Ohio surgeon to obtain medical records. Contact a Cincinnati hernia mesh lawyer to discuss potential hernia mesh injury lawsuits and settlement.

What hernia mesh products have allegedly caused injury?
  • Gore DualMesh
  • Aspide Surgimesh
  • Ethicon
  • Physiomesh
  • Proceed
  • Prolene
  • Covidien 
  • Parietex
  • Parietene
  • Permacol
  • Surgipro
  • Atrium
  • C-Qur
  • ProLoop
  • Bard/ Davol
  • Visilex
  • Composix
  • Marlex
  • Ventralight
  • Spermatex
  • 3D Max
  • Sepramesh
  • PerFix Plug
  • Ventralex
  • Kugel
How common is hernia recurrence?

Regardless of treatment, hernias have a high rate of recurrence, and surgeons often use surgical mesh to strengthen the hernia repair recurrence rate. The use of meshes is thought to reduce dramatically the incidence of hernia recurrence.

However, up to 50 percent of hernias may reoccur with an implanted device. This is commonly due to inadequate fixation during the original operation or shrinkage of the mesh. Light-weight meshes may have a higher risk due to their increased flexibility and movement.

Two-thirds of recurrences occur after three years. It is not clear if the type of mesh used has any effect on durability. All mesh products appear equally limited in effectiveness.

what are the different types of hernias?
  • Inguinal: occurs in the inner groin. The most common of abdominal hernias. Sometimes muscles that attach to the pelvis leave a weakened area and if there is a stress placed on that area, the weakened tissues can allow a portion of small bowel to slide through that opening, causing pain and producing a bulge. Inguinal hernias are more likely to occur in men.
  • Femoral: occurs in the upper thigh/outer groin. Femoral hernias tend to occur more frequently in women.
  • Incisional: occurs through an incision or scar in the abdomen. Incisional hernias occur as a complication of abdominal surgery, where the abdominal muscles are cut to allow the surgeon to enter the abdominal cavity to operate.
  • Ventral: occurs in the general abdominal/ventral wall
  • Umbilical: occurs at the belly button and are very common in newborns and often do not need treatment unless complications occur. Some umbilical hernias enlarge and may require repair later in life.
  • Hiatal: occurs inside the abdomen, along the upper stomach/diaphragm
  • Obturator: the least common hernia of the pelvic floor, mostly found in women who have had multiple pregnancies or who have lost significant weight.
How is a Medical Device Defined as Defective?

Ohio Definition of Defective

Under Ohio law, a medical device is  defective if it is unreasonably dangerous for its intended use. A legal cause of action can be based on several types of medical device product defects. Most jurisdictions a version of one or more of these cause of actions. 

(1)  Manufacturing/ Construction Defect of the medical device:

(2) Defective design and/or formulation of the medical device:

(3) Failure to warn or inadequate warning or instruction associated with the medical device:

(4) Misrepresentation on the Safety or Efficacy of the Medical Device:

(5) Fraud Related to the Safety or Efficacy of the Medical Device

(6) Negligent Distribution or Testing of the Medical Device

 

FAULTY MEDICAL DEVICES

Learn about Medical Device Approval Processes