VENTRALIGHT


Consumer Safety Lawyer investigates defective hernia mesh devices for injured plaintiffs nationwide
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Ventralight Hernia Mesh Lawsuits

reviewing mesh injury & complications

According to attorneys involved in handling recent hernia mesh injury and Ventralight lawsuit settlements, CR Bard and other medical device makers ignored available evidence and failed to undergo proper clinical testing in order to release unsafe hernia mesh products.

The Bard Ventralight ST hernia mesh product is a polypropylene mesh designed for use in hernia repair surgery. But the material used, polypropylene, has been known to expand and shrink after implantation, leading to infection, irritation, tissue damage and a dangerous foreign body response.

Bacteria can adhere to the mesh implant, compromising internal organs and delicate tissue. Polypropylene also tends to break down in the body over time, leading to patient complications, which may include:

  • Bowel Obstruction
  • Infection
  • Adhesion
  • Chronic pain
  • Hernia recurrence
  • Allergic reaction
  • Fluid buildup
  • Hematomas
  • Fistula formation
  • Tissue damage
  • Mesh erosion
  • Granuloma
  • Bowel Perforation
  • Need for revision surgery

Ventralight Complications

Patient complaints and adverse medical reports have shown that Ventralight mesh and other polypropylene mesh products present a health risk to consumers.

Yet, medical device manufacturers elected to release unsafe products at a huge consumer cost. Johnson & Johnson, Ethicon, Atrium, Aspide and Davol Bard have released hernia mesh products that have caused injuries and led to hernia mesh defect lawsuits.

The prevailing argument in the Ventralight lawsuit alleges that the product’s ST coating contributes to potential inflammatory reactions, infection and other side effects. Early signs of mesh implant failure include pain, discomfort, delay in healing, and heat radiating from the surgical site. Hernia mesh failure leads to complications and painful revision surgery.

Attorneys contend that there is scientific evidence that Bard should have known of that demonstrates their Ventralight ST mesh is incompatible with human tissue. Meanwhile, the company has made huge sums of money while litigation mounts.

Hernia mesh lawyers have file lawsuits based on claims of design defects, manufacturing defects, failure to warn, company negligence, breach of warranty, and violations of consumer protection laws.

Joe Lyon is a highly-rated Cincinnati, Ohio medical device attorney and hernia mesh injury lawyer representing plaintiffs nationwide in a wide variety of medical device recall lawsuits and and product liability cases.

Ventralight Mesh Lawsuits

Bard and other mesh manufacturers failed to warn consumers and surgeons of patient health risks. As a result, thousands of injured mesh implant patients are coming forward to file lawsuits against negligent medical device companies.

The use of hernia mesh implants can improve hernia patient outcomes. There is a known reduced rate of hernia recurrence, and many situations require the use of surgical mesh for hernia repair.

But when a defective mesh product is used, serious health risks endanger a patient.

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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 Ventralight 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 Ventralight 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.
What is a fistula?

Repair of hernias are done by either suture repair or prosthetic mesh repair. The latter is associated with a lower recurrence rate but a higher incidence of complications. The most serious complication is the development of fistula.

Fistula is a late complication of prosthetic mesh repair and is usually due to chronic erosion of bowel by mesh placed in direct contact with intestinal loops both in open and laparoscopic repairs. Symptoms of fistulas may include the following:

  •  Persistent pain—throbbing and worse when sitting down.
    •    Skin irritation around the anus, including swelling, redness and tenderness.
    •    Discharge of pus or blood.
    •    Constipation or pain associated with bowel movements.
    •    Fever
Does hernia mesh cause adhesions?

Hernia mesh adhesions are scar tissue resulting from hernia mesh operations and the healing process. Following hernia repair surgeries, adhesions may form in the abdomen or peritoneum. The mesh repairs usually heal quickly but when adhesions form, organs connected by the scar tissue may not function properly.

The popularity of hernia mesh operations has led to increasing concern regarding mesh-related adhesions. Adhesions result from the fibrin exudates that follow any kind of trauma.

These exudates form temporary adhesions until the fibrinolytic system absorbs the fibrin. Absorption is delayed in the presence of inflammation or foreign bodies such as mesh devices. In these situations, they develop into tissue adhesions.

All mesh implants produce adhesions, though their extent varies. Abdominal adhesions are a common complication, occurring in a majority of people who undergo abdominal or pelvic surgery. Adhesions cause the majority of small bowel obstructions in adults, and are believed to contribute to the development of chronic pelvic pain.

X-rays do not reveal potential mesh issues or diagnose the presence of adhesions. An additional surgery is usually needed to diagnose or treat hernia mesh adhesions. However, revision surgeries carry risks and can lead to further health problems, including infection, bowel blockage, bowel perforation and chronic pain.

Adhesions may begin forming long before they are noticed by patients or doctors. Depending on the location, adhesions from defective hernia mesh devices may cause pain and affect the bowel in different ways. Even removing a defective hernia mesh product may not completely solve all health issues.

Symptoms of adhesion and hernia mesh injury may include:

  •  Severe abdominal pain or cramping
    •    Vomiting
    •    Bloating
    •    Loud bowel sounds
    •    Swelling of the abdomen
    •    Constipation
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

 

Why should I hire The Lyon Firm?

Our Firm will help you find the answers.  The Firm has the experience, resources and dedication to take on difficult and emotional cases and help our clients obtain the justice for the wrong they have suffered. 

 Experience:  Joe Lyon is an experienced Cincinnati Defective Device Lawyer. The Lyon Firm has 17 years of experience and success representing individuals and plaintiffs in all fifty states, and in a variety of complex civil litigation matters. Defective device lawsuits can be complex and require industry experts to determine the root cause of an accident or injury. Mr. Lyon has worked with experts nationwide to assist individuals understand why an injury occurred and what can be done to improve their lives in the future. Some cases may go to a jury trial, though many others can be settled out of court.

Resources/Dedication: Mr. Lyon has worked with experts in the fields of accident reconstruction, biomechanics, epidemiology, metallurgy, pharmacology, toxicology, human factors, workplace safety, life care planning, economics, and virtually every medical discipline in successfully representing Plaintiffs across numerous areas of law. The Lyon Firm is dedicated to building the strongest cases possible for clients and their critical interests.

Results:  Mr. Lyon has obtained numerous seven and six figure results in medical device cases.  He has litigated cases successfully against some of  the largest companies in the world including:  Johnson & Johnson, Biomet, Ethicon, Stryker, Coloplast, Smith & Nephew, American Medical Systems, Boston Scientific, Medtronic, Guidant, Bard, & Bayer. 

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