Vaginal Mesh Recall

While many brands of surgical mesh, vaginal mesh, and bladder slings remain on the market, a few have been voluntarily recalled or discontinued. These include the Protegen Sling and ObTape, which was discontinued by its manufacturer in 2006.

In June 2012, another four vaginal mesh products were voluntarily discontinued, this time by the Johnson & Johnson subsidiary Ethicon: the Prolift, Prolift+ M, TVT Secur and Prosima systems. The medical device manufacturer Bard took its Avaulta mesh product off the U.S. market in July 2012.

If you received a vaginal mesh implant, a surgical mesh implant, or a bladder sling and you are suffering as a result, you might be able to recover compensation no matter what brand of mesh or sling your doctor used. To file a lawsuit for injuries you suffered as the result of a drug or medical device, that drug or medical device doesn’t have to have been recalled.

The Rottenstein Law Group is now accepting vaginal mesh lawsuit claims that concern all types of surgical mesh and vaginal mesh, whether or not those products have been recalled.

There Are Many Brands of Vaginal Mesh Still on the Market

Many brands of vaginal mesh are still on the market in the United States and Europe.

Victims of Many Mesh Brands Are Suing

Whether or not the particular brand of vaginal mesh they received has been recalled, victims of vaginal mesh injuries have filed lawsuits to obtain compensation for their injuries. They are suing several manufacturers, including Johnson & Johnson and Boston Scientific.

The federal cases against four vaginal mesh manufacturers—C.R. Bard; American Medical Systems; Boston Scientific; and Ethicon—have been consolidated into four multidistrict litigation (MDL) proceedings in the U.S. District Court for the Southern District of West Virginia, where District Court Judge Joseph Goodwin is presiding over pre-trial motions and discovery.

A fifth MDL is centralized in the U.S. District Court for the Middle District of Georgia. That one consolidates cases against Mentor Corp., the once-manufacturer of ObTape, a vaginal mesh product that is no longer on the market in the United States.

In addition to these MDL actions, there are two mesh mass torts pending in New Jersey state court: one against the manufacturer Bard and one against the manufacturer Gynecare.

MDL allows parties whose cases share common opponents, facts, and legal issues to combine their cases for the pretrial phase only. Consolidation saves the parties’ and the judiciary’s time and resources while allowing plaintiffs the opportunity to recover an amount of compensation that corresponds to their injuries, unlike in a class action lawsuit, which provides a fixed award. At the end of the pretrial process, the parties select a handful of plaintiffs, whose cases are typical of all plaintiffs, to try their cases before juries in what are called “bellwether trials.” Bellwether trials allow the remaining plaintiffs and defendants to assess their cases and decide whether they should proceed to trial themselves or settle out of court. The first vaginal mesh bellwether trial is scheduled to begin on February 15, 2013, against C.R. Bard.

Call Today For a Free Consultation

If you or someone you love has suffered from side effects or complications from a mesh implant, submit this simple secure form for a free and confidential evaluation to learn more about your eligibility to file a lawsuit.

Don’t let the type of mesh your doctor used affect your decision to contact us. Patients who have suffered from the side effects of all types of mesh are recovering.

Our lawyers understand the pain you’ve experienced. We will make the process of evaluating your claim as quick and simple for you as possible.

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rlg Previous Comments

  1. Guest
    on September 26, 2012 at 9:43 pm

    I received Hernia surgery in 2006. I have been to several doctors with complaints of pain, discomfort, and flared swollen scaring. I still have large amounts of pain at times as well as very sensitive to the area as well as some internal pain. Could this be a part of the mesh recall?

  2. Guest
    on July 17, 2012 at 4:54 pm

    Had surgery with mesh implant on Dec. 8, 2011 and 2 days later surgical site and mesh collapsed and tore. I needed to go to a wound care clinic for 3-4 months.

  3. Guest
    on June 6, 2012 at 9:50 am

    I had a hysterectomy in 2006 and the Dr. implanted me with a Gynzyme product. I ended up with an E. coli infection/abcess that had to be reached by going thru my butt muscle under CT with only local (I live in fear of that pain to this day). My sciatic nerve was hit and I endured horrors I'd like to forget. I had major pelvic pain and could hardly walk. I begged Drs. of all types to believe me and they ran multiple tests. I couldn't work, I was in my own private hell and I fell into a deep depression. Sex was excruciating --and my marriage began to suffer. I could hardly walk or take care of myself, let alone my two children. Even my closest family and friends began to doubt my pain and that was heartbreaking to me. Finally my Gastro Dr. referred me to a Pelvic Pain center where I was evaluated and it was determined that another surgery was needed to help "fix" some damage and scarring. I could tell immediately that something was a little better..no wonder.. I found out my Vaginal cuff was stuck to my colon and wall! Gee... I wonder why walking hurt like hell??!! There is more that I'm not going to go into here. My hope is that these products stop being used!

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