Sentences with phrase «surgical mesh»

The majority of surgical mesh devices currently available for use are constructed from synthetic materials or animal tissue.

Currently, there are more than 50 different surgical mesh products on the market.

In some cases, these problems were so severe that they required additional surgeries to repair problems with surgical mesh or to remove it entirely.

Several other companies have begun settling surgical mesh lawsuits for similar devices.

Many doctors say they don't have enough information on the long - term outcomes of surgical mesh surgeries.

Hundreds of surgical mesh patients have already filed lawsuits against the manufacturers of these products after suffering complications from the mesh.

Hundreds of women have filed lawsuits against the manufacturers of surgical mesh.

Transvaginal mesh is a type of surgical mesh device used for the treatment of pelvic organ prolapse or stress urinary incontinence.

On July 13, the FDA issued an update on a 2008 public health notification reporting complications from surgical mesh used in transvaginal mesh surgery are not rare.

In July 2011, the Food and Drug Administration issued a warning about the risk of complications with transvaginal surgical mesh products.

What she encountered left her dumbfounded: hundreds of patients talking about their problems with surgical mesh implants.

Hernia surgeries, as well, often use surgical mesh as part of the internal hernia repair.

Recently, Johnson & Johnson was ordered to pay a 64 - year - old woman $ 1.2 million for injuries she sustained from vaginal surgical mesh from its Ethicon line.

Proposed legislation currently in the House of Representatives would close that loophole by allowing the FDA to order additional safety studies on medical devices like surgical mesh before approving them.

According to the FDA, «the most frequent complications reported for surgical mesh devices for [pelvic organ prolapse] repair include mesh erosion through the vagina (also called exposure, extrusion or protrusion), pain, infection, bleeding, pain during sexual intercourse (dyspareunia), organ perforation, and urinary problems.»

Many surgical mesh manufacturers, including Johnson & Johnson and Bard, have voluntarily recalled transvaginal mesh products after increased patient complaints.

Pelvic organ prolapse (POP) and stress urinary incontinence (SUI) are often dealt with through surgical remedies involving inserting surgical mesh into the female's body to help and support the weakened area.

Many surgical mesh manufacturers have issued transvaginal mesh recalls after studies showed their products caused severe side effects.

Recently, the FDA made two proposals to tackle the risks involving surgical mesh and its use in transvaginal repair to treat pelvic organ prolapse.

Some of the potential complications of surgical mesh include pain, infection, bleeding, organ perforation urinary problems or vaginal mesh erosion at higher rates than patients who elect for traditional surgery.

Meanwhile, doctors insist surgical mesh is an important tool being unfairly maligned.

Public Citizen wants the FDA to require manufacturers to recall non-absorbable surgical mesh devices and future versions to be subject to more stringent approval requirements.

This new site details information regarding the brands of varying surgical mesh devices, research findings, explanations of the potential complications, and information regarding TVM lawsuits.

On July 13, 2011, the FDA warned physicians and patients of complications that could occur with the use of surgical mesh Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI) surgeries performed on women.

The FDA became concerned when it reviewed the published scientific literature from 1996 — 2011 to evaluate surgical mesh's safety and effectiveness.

Also referred to as surgical mesh protrusion, exposure, or extrusion, this problem involves the mesh device eroding through the vaginal wall, potentially causing infection, pain, bleeding, incontinence, painful sex, prolapse relapse, vaginal scarring, neuro - muscular issues, and vaginal shrinkage.

The FDA issued a new warning on July 13th 2011 regarding the use of synthetic surgical mesh to repair pelvic organ prolapse (POP).

The suit involved Ethicon Inc., and its parent Johnson & Johnson's Prolift surgical mesh device...

We've fought dangerous surgical mesh manufacturers, pharmaceutical companies that manufactured antibiotics that caused patients permanent nerve damage, and against the makers of Risperdal that caused thousands of males to develop gynecomastia.

Johnson & Johnson also sent notification of its decision to halt sales of the implants to judges that are overseeing surgical mesh lawsuits in New Jersey and West Virginia.

After receiving donations and support from the community, Sawyer recovered from the faulty surgical mesh and is volunteering for organizations that help others in need, including the Salvation Army.

If you or a loved one received a Johnson & Johnson surgical mesh device and have experienced complications, you may qualify for a lawsuit.

If you or a loved one have experienced pain or other complications after receiving a Boston Scientific surgical mesh device, you may be eligible to file a lawsuit.

This plastic, net - like material made of polypropylene, also known as urogynecologic surgical mesh, has caused health issues in thousands of patients.

The West Virginia surgical mesh trial is the first federal lawsuit to be heard in court, with more than 4,000 transvaginal mesh side effects lawsuits pending against C. R. Bard alone.

Other complications reported by surgical mesh users including severe pain, infection, sexual problems, urinary problems, bleeding and organ perforation.

Though the vast majority of surgical mesh procedures transpire without incident, the few that result in complications can cause serious, lasting, and far - reaching damages.

If you or a loved one have experienced pain or other complications from a Gynecare surgical mesh device, you may be eligible to file a lawsuit, for a free legal consultation, contact the lawyers with Hissey Kientz, LLP by calling us toll - free at 1-866-275-4454, or by filling out the free case evaluation form located on this page.

If you or someone you love was treated with a Covidian surgical mesh product and has experienced problems with the device, you may be eligible to file a lawsuit.

Please visit our complete list of surgical mesh brands for more information about other transvaginal mesh products.

If you or someone close to you has experienced problems after receiving an Ethicon surgical mesh product, you may qualify to file a lawsuit.

In September 2011, an advisory committee voted to recommend that the FDA upgrade the warning classification for surgical mesh because of the risk of side effects associated with the device.

If you or a loved one received a Mentor surgical mesh product and have experienced complications, you may be eligible to file a lawsuit.

If you or a loved one received a Tyco surgical mesh device and have experienced pain or other problems, you may be eligible for a lawsuit.

Products including artificial joints and surgical mesh sometimes make it past the FDA before sufficient testing is conducted or design defects are discovered.

The agency stated that it had received thousands of reports since 2005 of complications regarding transvaginal surgical mesh products, many of which required surgery or hospitalization.

If you or a loved one had surgical mesh implanted for Pelvic Organ Prolapse (POP) or Stress Urinary incontinence (SUI), you may be entitled to compensation for your injuries.

Companies could face thousands of surgical mesh lawsuits after the first transvaginal mesh lawsuit to go to trial resulted in the patient receiving $ 11 million from a jury.

The Food and Drug Administration issued a warning in July 2011 about complications experienced by women who have undergone treatment with surgical mesh products.