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PROLOOP


Medical Device Lawyer investigating ProLoop Hernia Mesh Injury for plaintiffs nationwide
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ProLoop Hernia Mesh Lawsuits

investigating mesh device complications & Injury
Thank you for considering The Lyon Firm. At this time, we are not accepting plaintiffs related to this specific consumer issue. However, if you would like to be contacted in the future, please complete the contact form. By completing the form you will be contacted if the Firm begins accepting new cases on this matter, and you will also be included in firm news alerts related to important consumer safety and privacy issues to help keep you informed about related issues.

Thousands of hernia mesh implant recipients across the country have been injured and required revision surgery. Patients hoping to improve their quality of life instead are faced with severe injuries, including infections, chronic pelvic pain, adhesions, fistula, and other complications. Patients injured by a Proloop mesh device should contact an attorney. 

Medical device companies, including Bard, Ethicon, Gore and Atrium have allegedly produced and distributed unsafe hernia mesh products, and failed to properly warn patients of the numerous risks and complications associated with the mesh implants.

A number of hernia mesh and pelvic mesh implants have been recalled, and the U.S. Food and Drug Administration (FDA) has issued warning regarding certain products, including Atrium’s ProLoop mesh implant.

ProLoop Hernia Mesh injury

Patients who have have revision surgery or mesh replacement surgery from June 2010 to February 2015 and experienced any of the following should contact a hernia mesh attorney to review your case:

  • Chronic pain
  • Recurrent hernia
  • Seroma
  • Adhesion
  • Infection
  • Granuloma
  • Foreign Reaction to mesh
  • Bowel Obstruction

Joe Lyon is a highly-rated medical device defect lawyer and product liability attorney reviewing Hernia Mesh Injury cases for injured plaintiffs nationwide.

The Lyon Firm represents clients on a contingency fee basis and seeks maximum compensation following injuries due to corporate negligence and failures to warn consumers of potential health risks

Atrium Hernia Mesh

Due to negligent design, many mesh implant recipients have experienced serious injury and complications. Revision surgery and permanent injury are not as uncommon as many think. As a result, many industry experts and consumer safety attorneys have stood by injured plaintiffs and filed hernia mesh defect lawsuits.

Compensation can be recovered to help cover medical expenses, pain and suffering, long-term disability, lost wages as well as punitive damages.

Atrium ProLoop Lawsuits

Atrium manufactures a number of different hernia mesh products, some of which have allegedly caused injury. C-QUR and ProLoop products have seen reported injury and complications,  as well as the following:

  • C-QUR TACSHIELD, V-Patch, Centrifx, FX: includes sheets of polypropylene, coated with omega 3 fatty acids.
  • PROLOOP: 3D mesh plug made of polypropylene.
  • PROLITE and PROLITE ULTRA : flat sheet made of polypropylene monofilament.

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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 proloop lawsuits
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 ProLoop Mesh Litigation

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
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. 

FAULTY MEDICAL DEVICES

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