Vaginal Mesh Class Action Lawsuit | Get the Right Lawyer

Females who suffered serious injuries following the implantation of surgical mesh for pelvic organ prolapse (POP) or stress urinary incontinence (SUI) might need to seek out a lawyer specializing in vaginal mesh cases. Over the past few years, there have been numerous reports linking mesh devices to a range of adverse effects such as erosion, infections, pain, painful sexual intercourse, damage to internal organs, and the return of POP and SUI symptoms. Often, these issues related to vaginal mesh are irreversible and can impact a woman’s wellbeing permanently.

Update: New Jersey Jury Awards Plaintiff $68 Million in Bard Mesh Lawsuit

April 20, 2018 – A jury in Bergen County, New Jersey, has awarded $68 million ($33 million in compensatory damages and $35 million in punitive damages) to a woman who claims she was severely injured by C.R. Bard’s Avaulta Solo Support and Align Trans-Obturator Urethral Support Systems. Plaintiff Mary McGuinness was awarded $23 million in actual damages and her husband Thomas was awarded $10 million for loss of consortium, according to court documents.

Free Vaginal Mesh Lawyer Evaluation: If you or a loved one has been injured or suspect that you may have complications directly linked to the placement of a vaginal mesh product, you should contact our law firm immediately. You may be entitled to compensation by filing a suit against the manufacturer of the vaginal mesh and we can help.

What’s the Problem?

In recent years it has come to the public’s attention that women who undergo POP or SUI treatment with mesh products are at an increased risk of developing a number of adverse health complications compared to women who are treated with more conventional methods. To date, the FDA has received nearly 4,000 reports of vaginal mesh complications including:

• erosion through vaginal epithelium
• infection
• pain, including dyspareunia
• urinary problems
• recurrence of prolapse and/or incontinence
• bowel, bladder perforation, and blood vessel perforation
• vaginal scarring
• mesh erosion

FDA Warning on Vaginal Mesh

In October 2008 and February 2009, the U.S. Food & Drug Administration (FDA) issued public health notifications regarding the use of vaginal mesh devices for the treatment of women’s urinary problems. These notifications were issued after the FDA received over 1000 injury reports associated with surgical mesh. Then in July 2011, the administration issued an update stating that it had received a number of additional reports of serious side effects suffered by women implanted with vaginal mesh devices. Specifically, the FDA stated:

i). Complications related to transvaginal mesh surgery are NOT rare; (ii) There is no evidence that transvaginal mesh repair is more effective than traditional non mesh repair; and (iii) Transvaginal mesh surgery exposes patients to greater risk than traditional non mesh repair.”

Vaginal Mesh Surgery Considerations

If you are suffering from pelvic organ prolapse or stress urinary incontinence, and are considering vaginal mesh surgery, the FDA advises you to consult your healthcare provider about all treatment options before making your decision. If you elect to undergo the procedure, you should continue with check-ups and follow-up care after surgery. Contact your doctor right away if you begin suffering from any of the complications listed in this article. Women who have had POP or SUI surgery but don’t know if the surgeon used mesh should find out if it was used during their next scheduled visit with their doctor. The vaginal mesh lawyers at Schmidt & Clark, LLP, are accepting potential lawsuits against devices made by Johnson & Johnson, Bard, American Medical Systems (AMS), and Boston Scientific.

Kentucky AG Sues J&J Over Defective Marketing of Vaginal Mesh

August 17, 2016 – Kentucky’s attorney general Andy Beshear is suing Johnson & Johnson for millions of dollars, saying the company “concealed and misrepresented” the risks of its transvaginal mesh products to the public and medical communities. Beshear said over 15,000 women in Kentucky had transvaginal mesh implanted but J&J, through its medical device company, Ethicon, didn’t provide enough information about adverse effects.

FAQs

Are there any FDA warnings regarding vaginal mesh?

Yes, the FDA has issued warnings and safety communications regarding vaginal mesh, highlighting the risks of complications such as mesh erosion and organ damage. These warnings are crucial evidence in lawsuits as they establish known risks associated with the device.

How long do I have to file a vaginal mesh lawsuit?

The time limit to file a vaginal mesh lawsuit, known as the statute of limitations, varies by state. It’s crucial to consult with a lawyer promptly to ensure your claim is filed within the legal timeframe to preserve your rights.

Can I join a class action lawsuit if I was affected by vaginal mesh?

Yes, individuals affected by vaginal mesh complications may join a class action lawsuit if one is available. Class action lawsuits allow multiple plaintiffs to combine their cases, providing a stronger collective legal action against the manufacturer.

Related Article: Ethicon Transvaginal Mesh Recall Suit

See the other medical device lawsuits our lawyers are currently accepting.

Do I Need a Vaginal Mesh Lawyer?

The Medical Device Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in vaginal mesh lawsuits. We are handling individual litigation nationwide and currently accepting new vaginal mesh complications cases in all 50 states.

Free Confidential Case Evaluation: Again, if you were injured or suspect that you may have complications directly linked to POP or SUI surgery and/or the placement of a vaginal mesh product, you should contact our law firm immediately. You may be entitled to compensation by filing a suit and we can help.