Posts Tagged ‘New Jersey’

New News For The Bard Vaginal Mesh Lawsuits

Written by Vaginal Mesh Helpline on . Posted in Austin Vaginal Mesh lawyers, Dallas Vaginal Mesh Lawyer, Fort Lauderdale vaginal mesh lawyer, Houston Vaginal Mesh Lawyer, Miami, Fort Lauderdale, West Palm Beach Vaginal Mesh Lawyer, Orlando, Jacksonville, Tampa Vaginal Mesh Lawyers, Pelvic Mesh Lawsuit, Vaginal Mesh News

Vaginal Mesh Helpline will keep you up to date on all the latest news  from vaginal mesh lawyers on the vaginal mesh lawsuit trials. This is the latest news on the Bard vaginal mesh trials.

Bard  Has Limited The  Plaintiffs’ Expert Testimony In  The Vaginal Mesh MDL Lawsuit

MDL No. 2187 | In RE: CR Bard, Inc., Pelvic Repair System Products Liability Litigation

C.R. Bard’s products include:

  • Bard Pelvitex
  • Bard Pelvisoft
  • Bard Pelvilace or Pelvicol
  • Bard Utrtex
  • Bard Uretex TO
  • Bard Uretex TOO2
  • Bard Uretex TOO3

Law360, New York (June 06, 2013, 8:08 PM ET) — A West Virginia federal judge on Tuesday excluded or limited the testimony of the plaintiffs’ experts targeted by C.R. Bard Inc. in four bellwether cases in multidistrict litigation over injuries allegedly caused by the company’s vaginal mesh products.

U.S. District Judge Joseph Goodwin also granted a substantial portion of Bard’s motions for partial summary judgment as to the plaintiffs’ claims in the four cases. The bellwethers are scheduled to go to trial July 8.

Ethicon Mesh Lawyers, Gynecare Mesh Lawsuit Updates and News

Written by Vaginal Mesh Helpline on . Posted in Dallas Vaginal Mesh Lawyer, Fort Lauderdale vaginal mesh lawyer, Houston Vaginal Mesh Lawyer, Houston-Vaginal Mesh Lawsuits, Miami, Fort Lauderdale, West Palm Beach Vaginal Mesh Lawyer, Orlando, Jacksonville, Tampa Vaginal Mesh Lawyers, Pelvic Mesh Lawsuit, Pelvic Mesh Lawyer, Transvaginal Mesh Lawyer, Vaginal Mesh lawsuit Lawyer, Vaginal Mesh Lawyer Fort Lauderdale, Vaginal mesh Lawyers, Vaginal Mesh News

The vaginal  mesh lawsuits for the  Ethicon Inc.’s Gynecare pelvic mesh have been consolidated  in New Jersey’s Atlantic County Superior Court. These mesh products appear to have been broadly used for urinary incontinence in women.   A Case Management Conference was held on May 22nd to discuss  issues stemming from the proceeding’s first trial, which concluded in March with an award of more than $11 million for a woman mesh  victim.  The Vaginal Mesh Helpline is glad to see that the mesh trials are moving along and advises all women to file their Gynecare, Ethicon vaginal mesh lawsuit.(In re: Pelvic Mesh/Gynecare Litigation, No. 6341-10)

“As the  Vaginal Mesh Helpline  medical social worker I am  happy to see more progress in  the vaginal mesh lawsuits.  I speak to women on a daily basis implanted with Ethicon vaginal mesh and  are suffering from  serious, life-changing complications due to these mesh implants.”

Vaginal Mesh lawyer Network Formed

The Vaginal Mesh Helpline has formed a nationwide lawyer network to help represent victims of defective vaginal mesh devices. We want to hear from the victims of Ethicon vaginal mesh failure.

Transvaginal Mesh Lawsuits 

The  Ethicon mesh lawsuits  have been mounting. Most women we speak to have had these implanted for   urinary incontinence. In  July 2011, the U.S. Food & Drug Administration (FDA) warned that there had been an   increase in vaginal mesh complications reported to them.

 Vaginal Mesh News And Updates

The first bellwether trial in the New Jersey C.R. Bard litigation will begin on September 23, 2013, and will involve a vaginal mesh device used to treat pelvic organ prolapse. (In re: Pelvic Mesh Litigation/Bard, No. L-6339-10) The first trial will involve a product manufactured by C.R. Bard, is scheduled to begin in June.

  • American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2325”)
  • Boston Scientific Corp., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2326)
  • C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2187”)
  • Ethicon, Inc., Pelvic Repair Systems Products Liability Litigation (“MDL No. 2327”)

We strongly suggest all women file their vaginal mesh lawsuits right away.

Vaginal Mesh Lawsuits Proceed, Vaginal Mesh Helpline Applauds

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

Vaginal Mesh Helpline shares all the latest news regarding the vaginal mesh, pelvic mesh lawsuits and updates from vaginal mesh lawyers regarding the proceedings.

Vaginal mesh lawsuits  involving Prolene mesh  products manufactured by C.R. Bard, Inc., continue to move proceed in a multidistrict litigation  U.S. District Court, Southern District of West Virginia.  In an Order issued on May 17th, the Court denied a request by C.R. Bard to seal emails that included supplier information the company claimed would reveal trade secrets and other confidential, proprietary information about its suppliers. The emails were filed as exhibits by plaintiffs in response to certain motions made by Bard, according to the Order. (In re: C.R. Bard, Inc., Pelvic Repair Systems Products Liability Litigation – MDL No. 2187). Other lawsuit are also progressing for vaginal mesh complications against American Medical Systems, Inc., C.R. Bard, Inc., Ethicon, Inc. and Boston Scientific Corp.

 Prolene  Mesh  Lawsuits West Virginia

C.R. Bard is only one of the manufacturers for which consolidated lawsuits are underway in the Southern District of West Virginia  under Judge Goodwin. The first bellwether trial in the C.R. Bard multidistrict litigation is scheduled to begin in June, and will involve a Bard Avaulta transvaginal mesh lawsuit. Other litigations underway in West Virginia include In re: American Medical Systems, Inc., Pelvic Repair Systems Products Liability Litigation – MDL No. 2325; In re: Boston Scientific Corp., Pelvic Repair Systems Products Liability Litigation – MDL No. 2326; and In re: Ethicon, Inc. Pelvic Repair Systems Products Liability Litigation – MDL No. 2327. The Vaginal Mesh Helpline is watching for continuous updates and will keep you posted.

 Prolene Mesh Lawsuits In New Jersey

More C.R. Bard and other manufacturer vaginal mesh lawsuits have been consolidated in New Jersey Superior Court, Atlantic County. The first trial will begin in September 2013. (In re: Pelvic Mesh Litigation/Bard, No. L-6339-10, and). We also have Ethicon transvaginal mesh lawsuits here as well (In re: Pelvic Mesh/Gynecare Litigation, No. 6341-10) One of the ones we see in the news is (Gross v. Gynecare Inc., Atl-L-6966-10, Superior Court of Atlantic County, New Jersey). Gross filed a vaginal mesh lawsuit and was awarded just over $11 million for her  suffering.

Victims  the Prolene vaginal mesh, Transvaginal Mesh, Bladder Sling, TVT, Pelvic mesh and all vaginal mesh products causing  complications  should contact us immediately to discuss their rights and get support a lawyer or a doctor.

Vaginal Mesh Lawyers Filing Nationwide Vaginal Mesh Lawsuits

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

Vaginal Mesh helpline, vaginal mesh lawyers are filing lawsuits for women injured by the vaginal mesh. If you have been rejected due to the statute of limitations or other criteria call the Vaginal Mesh Helpline to speak to one of our experienced mesh lawyers today.

The vaginal mesh lawsuit bellwether trials have begun and the mesh lawsuits are heating up. You must file your mesh lawsuit immediately.

What are the Transvaginal Mesh Complications ?

  • Erosion of vaginal tissue can result from a vaginal mesh
  • Hardening of the vaginal mesh
  • Infection is a serious mesh-patch complication
  • Pain and discomfort
  • Perforations of the bowel, bladder or blood vessels
  • Recurrence of Pelvic Organ Prolapse (POP) and Stress Urinary Incontinence (SUI)
  • Urinary problems and more severe incontinence
  • Painful sexual intercourse
  • Potential injury to the partner
  • Feeling the mesh or pieces of substance in the vaginal canal
  • Vaginal mesh erosion
  • Increased incontinence
  • Lower back pain
  • Abdominal pain
  • Gastrointesitnal discomfort
  • Bladder and or bowel incontinence
  • Difficulty voiding and the need for self catherizations
  • Vaginal scarring

Vaginal Mesh Lawsuits Are  Against These Manufacturers

  • C.R. Bard’s Avaulta
  • Ethicon’s Gynecare
  • American Medical Systems’ products:
  • AMS Apogee
  • AMS BioArc
  • AMS Elvate
  • In-Fast Unltra
  • MiniArc
  • Monarc
  • AMS Perigee
  • SPARC
  • Straight-In mesh
  • Boston Scientific Scimmed’s Pinnacle pelvic mesh
  • Covidien
  • Sofradim
  • Caldera
  • Mentor Corporation

To file a vaginal mesh lawsuit call us today.

 

Yaz Birth Control Pills Lawyers, New April 2012 Warning Date, Yaz Lawyers Filing Yaz Lawsuits

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh Information

The VaginaL Mesh Helpline is keeping women updated on all dangerous drugs and devices harming women. Many women were injured by Yaz  birth control pills and thought that they were out of luck in filing a Yaz lawsuit. Yaz complications  include: Blood clots, stroke, pulmonary embolism, deep vein thrombosis and in some instances death. Many women with complications and families that have lost loved ones due to Yaz felt they could not file a lawsuit. But, new warnings issued in April pf 2012 has opened doors for an influx of Yaz lawsuits. We do not want you to be left out.

The FDA Ordered  Warning Label Changes For  Yaz Blood Clots

The FDA announced it was requiring a label change for  Yaz

On April 10, 2012, the FDA announced it was requiring a label change for Yaz which contains Drospirenone. This warning   announced that Yaz may be associated with a higher risk for blood clots due to Drospirenone. This warning date may mean you now have a Yaz lawsuit even though you may have been turned away before.

Yaz  Lawsuit Complications

  • Blood Clot
  • Stroke
  • Pulmonary embolism
  • Deep Vein Thrombosis

Blood clots from Yaz may be linked to an increased risk of stroke, deep vein thrombosis and pulmonary embolism injuries to the lungs.

A federal Multi-District Litigation court in Illinois set up to handle lawsuits filed over alleged Yaz side effects has reported more than 10,000 cases filed. The formal case is known as Yasmin and Yaz (Drospirenone) Marketing, Sales Practices and Products Liability Litigation (MDL No. 2100).

Yaz lawsuit lawyers are accepting lawsuits from women who have have suffered these  side effects after taking Yaz. Yaz blood clots have caused premature death in young women. This is another medical product that targets women. Women must stand up and demand justice.

Stryker Hip Replacement Effects Women More, Stryker Hip Replacement Lawyers For Women

Written by Vaginal Mesh Helpline on . Posted in Stryker Hip Replacment lawyer for Women, Vaginal Mesh News

The Vaginal Mesh Helpline continues it it’s mission to inform about all dangerous drugs and devices harming women. It appears that even the recent hip replacement recalls effect women more then men. When will women stop being the target of these manufacturers? The vaginal mesh has caused severe injury. Just today we received a call from a woman about her mother of 76 who must wear a colostomy bag after mesh removal. And now the FDA reports that these metal on metal and metal component hip implants  put women at a higher risk. Both the Stryker Rejuvinate and ABG II are  dangerous surgical implants that have a greater failure rate and complications for women.

Many articles and reports have been released that discuss hip replacements having a greater failure rate in women.

Hip replacements like Stryker Rejuvinate and ABG II are slightly more likely to fail in women than in men, according to research published Monday in JAMA Internal Medicine.  The research was financed by the Food and Drug Administration. Another report discusses hip resurfacing and states a drawback for women because of the bone weakening that accompanies menopause. Meanwhile, even advocates of resurfacing acknowledge that they have yet to agree on how best to screen women for the procedure.

“We were surprised by the results, as studies suggest that larger heads should have  lower wear and a lower risk of dislocation. However, we have seen an increase in revisions for pain and loosening, particularly in women,” says Alison Smith, a study author and statistician at the University of Bristol in the U.K. Depending on patient age and implant head size, the revision rate for all-metal hips is three to four times higher in women and two to three times higher in men compared with other implants.

The FDA Reports Women At a Higher Risk For Failure

The Food and Drug Administration, along with its safety communication, has included a list of risk factors that can increase a patient’s chances of suffering from metal on metal hip implant complications. Patients who are overweight, female, or physically active are more likely to suffer complications related to these hip replacement systems, and patients who have a sensitivity to certain metals, have kidney failure, have a suppressed immune system, or take corticosteroids are also more at risk.

It seems women are always the victims for these manufacturers that choose profits over warnings.

Hip Replacement Failure More Likely In Women, Study Says Studies on Google News Today

Hip replacements are more likely to fail in women than in men, but the overall risk of implant failure is low–according to a study published in the Journal of the American Medical Association, JAMA, and that was funded by the U.S. Food and Drug Administration.

Women account for the majority of the more than 400,000 patients who undergo either full or partial hip replacements in the U.S. each year.

“This is the first step in what has to be a much longer-term research strategy to figure out why women have worse experiences,” said Diana Zuckerman, president of the nonprofit National Research Center for Women & Families.

It appears the smaller frame and difference in the curve of the hip and pelvic region accounts for this. Anatomy appears to play a role.  Women tend to have smaller joints and bones than men, and so they tend to need smaller artificial hips. Devices with smaller femoral heads  the ball-shaped part of the ball-and-socket joint in an artificial hip are more likely to dislocate and require a surgical repair.

I wonder why there cannot be two types of replacements, one for women and one for men. But, since they are all being recalled it would just mean more injured women. I am sure there would be extensive marketing to hook women in explaining how their lives would remain active and have a better quality. If you or a wife, mother, girlfriend or female loved one has been injured by these hip implants contact us and we will direct you to a Stryker Hip Replacement lawyer.

 

 

 

 

Mesh Lawyers are Filing Nationwide Mesh Lawsuits, The Mesh Trials Have Begun

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

The Vaginal Mesh Helpline announces the mesh trials have begun. Mesh lawyers are filing mesh lawsuits in droves. The quantity is increasing daily. Soon we will see justice. We all know the monetary compensation will never be enough for the agonies I have heard from our callers but, it is a first step. The FDA has not removed the mesh from the market even to this date. We must send a message to these mesh manufacturers.

We will keep you posted on the  mesh lawsuit  with mesh trial updates

Many  makers of Mesh Implants have faced their first jury trials and the outcome was seven figure jury awards for women victims these cases. Mesh implant manufacturers face a large number of mesh lawsuits. We also want to remind women, if you have had the mesh removed you should get the mesh for preservation.

we have been listening to women for months about their mesh complications. Remember a mesh is a mesh:

Transvaginal Mesh,  or pelvic mesh, or  bladder sling, whatever product you want to call it, it is a Prolene mesh. The goal of our mesh helpline has been to reach any woman who has suffered a severe injury as a result of complications with a mesh Implant and help them file a  Mesh Lawsuit. In addition, husbands, children,and family  members of women may sue for wrongful deat and loss of consortium.  We want to hear from you.

 

 

 

 

 

 

FDA Approves Over The Counter Medication For Overactive Bladder, Vaginal Mesh Helpline Reports

Written by Vaginal Mesh Helpline on . Posted in Medical News and Your Vaginal Mesh, Vaginal Mesh News

At the Vaginalmeshhelpline.com we are always looking for new information to help our readers injured by the vaginal mesh. Many women have had the mesh implanted for urinary  incontinence. We just found this online and are sharing it. The FDA has  approved  Oxytrol for women.  This is an over-the-counter Oxytrol treatment for overactive Bladder. Of course we suggest discussing this with your doctor.

January, 25, 2013 — The U.S. Food and Drug Administration today approved Oxytrol for Women, the first over-the-counter treatment for overactive bladder in women ages 18 years and older.

Oxytrol will remain available for men with overactive bladder by prescription only.

Overactive bladder is a condition in which the bladder squeezes too often or squeezes without warning. Symptoms include leaking urine (urinary incontinence), feeling the sudden and urgent need to urinate, and frequent urination. Overactive bladder affects an estimated 33 million Americans, the majority of whom are older women.

Oxytrol for Women contains oxybutynin, a medicine that helps relax the bladder muscle. Oxybutynin belongs to a class of drugs known as anticholinergics. It is the first drug in this class to be made available over-the-counter for treatment of overactive bladder.

Oxytrol for Women is a patch that is applied to the skin every four days. The patch delivers 3.9 milligrams of oxybutynin per day.

 

“Studies demonstrate that over-the-counter Oxytrol for Women is a safe and effective treatment for overactive bladder,” said Shaw Chen, M.D., Ph.D., deputy director of the Office of Drug Evaluation IV in the FDA’s Center for Drug Evaluation and Research. “Women should make sure to follow the Drug Facts label and consult their doctor if their condition does not improve.”

 

Oxytrol for Women’s safety and effectiveness for over-the-counter use were established in more than 5,000 subjects participating in nine studies. Overall, results from these studies showed that consumers can understand the information on the label, properly select whether the product is right for them, and use the drug appropriately.

Side effects reported during clinical studies were mild and included skin irritation where the patch was applied, dry mouth and constipation. A leaflet with tips to help manage overactive bladder will be provided with the product.

Oxytrol for Women is marketed by Merck, based in Whitehouse Station, N.J.

Source: FDA

Posted: January 2013

A Vaginal Mesh is A Transvaginal Mesh is A Bladder Sling is a Horror Story

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

They come under so many names manufactured by dozens of manufacturers but, the are all Prolene mesh and over 300,000 women have had them implanted. Some where aware of the implantation and others were just going in for a hysterectomy and came out with a mesh.

You have seen it on T.V and the lawsuits are being filed by the thousands as a multi district litigation consolidated in West Virginia for the most part. They are called a vaginal mesh, TVT sling, Transvaginal mesh, TVT, Bladder sling, pelvic mesh, Prolene mesh, surgical mesh, Bladder Neck Suspension Kit, SPARC Sling, MiniArc, Avaulta System, ProteGen Sling, ObTape, Desara Sling, IVS Tunneller I, Gynecare Prolift, TVT, Transvaginal Surgical mesh, Gynemesh, Polyform mesh, Apogee System, Perigee System, Pinnacle, and Advantage cystocele mesh, rectocele mesh, and are used for organ prolapse or urinary incontinence. Some women have one, some have two and some have three. Many have tried to get it removed only to find a new one has taken it's place. Women are in agony. Many can no longer work and others have seen their marriages fall apart. This Prolene mesh of many names makes it impossible to have rerlations without pain. Many women describe it as a knife cutting all the time. This is quite understandable as these synthetic plastic mesh placed inside a womens pelvic area are falling apart and eroding thru the vaginal wall. Many are eroding into the bladder and bowel causing a dangerous medical situation.

This mesh of many names has very severe complications. It can erode right thru the vaginal wall into the vaginal canal. Erode in it's simplest terms means cut right thru. The mesh causes relentless pain and infections that never stop. Many women have been on antibiotics for months on end which in and of itself is dangerous. The mesh can cause bleeding and the return of incontinence and prolapse with a vengence. This can be incontinence and re prolapse of the bladder or the bowel. There can be gastrointestinal problems, lower back pain, pain on one side, leg pain, neurological issues and the result is lives destroyed and severe emotional and psychological problems.

This mesh of many names has caused deaths. Some of these do to medical reasons and some do to choice in reaction to a sense of victimization that there appears to be no end to. Doctors are not listening, and if they have found one there is no longer insurance or funds for surgery. We have talked to women of all ages from 33 to 86. Who would put a mesh into a senior or a women still intent on having children is beyond me. We have spoken to women who have become pregnant with a piece of prolene mesh right there waiting for child birth. Some of it failing apart internally right in the pelvic region with very sharp edges.

With all the warnigs, stories and lawsuits the FDA has not recalled the mesh and many doctors are still putting it in. They believe the ones they put in will not fail. These are just not the ones that are falling apart. Somehow they are the magic doctor. Johnson and Johnson has pulled most of their Gynecare mesh products off the market under the Ethicon label and changed the labeling on one for warnings against vaginal implantation. However, this was just a business decision they say.  There was nothing wrong with the mesh at all.

Many names  yet, all a vaginal mesh.

  • A Mesh is A Mesh Is A Mesh
  • Pelvitex
  • Pelvisoft
  • Pelvilace or Pelvicol
  • Utrtex
  • Uretex TO
  • Uretex TOO2
  • Uretex TOO3
  • A Mesh is a Mesh is A Mesh     
  • TVT Exact
  • TVT Abbrevo
  • TVT Retropubic System
  • TVT
  • TVT Obturator
  • TVT Secur
  • Gynemesh PS
  • Prolift
  • Prolift+M
  • MiniArc Precise Single-Incision Sling
  • MiniArc Single Incision Sling
  • Monarc Subfascial Hammock
  • In-Fast Ultra Transvaginal Sling
  • BioArc
  • Sparc Self-Fixating Sling System
  • Elevate
  • Perigree
  • Apogee
  • Arise
  • Tyco Covidian Duo
  • Mentor ObTape
  • Coloplast Mesh
  • Pinnacle
  • Advantage Fit
  • Lynx
  • Prefyx PPS
  • Scientific Solyx

So many names, so many mesh so much pain and so much suffering.

If you have one of these mesh under so many different names it is still a mesh and you must come forward and fill your pelvic ,msh lawsuit immediately. The statute of limitations is running close. We cannot let anyone be left out. These mesh manufacturers must hear your voices and just must be sort for women everywhere with a mesh.

Coloplast Vaginal Mesh Lawsuits, Coloplast Vaginal Mesh Lawyer

Written by Vaginal Mesh Helpline on . Posted in Vaginal Mesh News

Vaginal Mesh Helpline is seeking women nationwide with a coloplast vaginal mesh to assist with locating a vaginal mesh lawyer for the Coloplast MDL vaginal mesh lawsuit. Leader ship roles have been assigned for lawyers in the coloplast MDL litigation.

Updated News On the Coloplast Vaginal Mesh

October 1, 2012 — Judge Joseph R. Goodwin has assigned leadership roles in the newly-formed Coloplast vaginal mesh Multidistrict Litigation (MDL). Three attorneys have been assigned Co-Lead Counsel roles on behalf of plaintiffs who were injured by Coloplast vaginal mesh. The MDL is currently located in the U.S. District Court for the Southern District of West Virginia.

After an MDL is formed, one of the first steps is assigning attorneys to play leadership roles. The Coloplast MDL was formed on August 6, 2012, by the U.S. Judicial Panel on Multidistrict Litigations (JPML). The JPML has assigned several vaginal mesh MDLs to Judge Goodwin’s court. The other MDLs are against manufacturers Johnson & Johnson (Ethicon), C.R. Bard, American Medical Systems, and Boston Scientific.

Judge Goodwin has already assigned leadership roles in the other MDLs. This includes a massive Plaintiffs’ Steering Committee, which involves 60 attorneys assigned various duties. He has also assigned several attorneys to coordinate common issues among the five MDLs. There may be matters of fact and legal issues that are common to the various litigations, and coordinating these issues may expedite the litigation.

Judge Goodwin has expressed his desire to expedite the Coloplast MDL as much as possible, to catch up with the other MDLs that are already proceeding.

On September 21, Judge Goodwin assigned three attorneys to serve as Co-Lead Counsel in the Coloplast litigation. One of these attorneys was  Mark Mueller, od Austin Texas. He  will have many responsibilities in the litigation, including speaking for plaintiffs during pre-trial proceedings, submitting and arguing motions, examining witnesses, introducing evidence, and more.

Coloplast Vaginal Mesh, Transvaginal Mesh Products

 

  • Novasilk – Synthetic Flat Mesh
  • Suspend – Tutoplast Processed Fascia Lata
  • Suspend – Tutoplast Processed Fascia Lata
  • Exair – Prolapse Repair System
  • Exair – Prolapse Repair System
  • Axis – Tutoplast Processed Dermis
  • Axis – Tutoplast Processed Dermis
  • Restorelle Smartmesh – Prolapse Repair System
  • Restorelle Smartmesh – Prolapse Repair System

SUSPEND VAGINAL MESH ALSO KNOWN AS A TRANSVAGINAL MESH: This is made from biologic human material and claims to integrate nicely into the human body to adequately treat POP, with little to no complications.

AXIS VAGINAL MESH: This is another product made from biologic material taken from the back of the leg. Again, they claim that it integrates well into the body to treat POP adequately.

NOVASILK VAGINAL MESH: This is a synthetic Transvaginal Mesh used to treat several types of POP. They claim that there are fewer complications because there is less material implanted than with other meshes.

EXAIR VAGINAL MESH: This is a polypropylene mesh used to reinforce a prolapsed pelvic floor.