Transvaginal mesh, also known as a surgical mesh, is a synthetically or biologically manufactured implant. Inserted through the vagina, a fact that also lends it its name, it is meant to the address pelvic organ prolapse (POP) and/or stress urinary inconsistence (SUI). Like other surgical implants, the transvaginal mesh too has side effects, causing severe pain and injury.
Transvaginal Mesh Recalls and their Causes
Since the product has not lived up to its purpose in a number of cases, therefore it has prompted the U.S. Food and Drug Administration (FDA) to issue warnings and alerts on the possible dangers associated with mesh. In 2008, the FDA issued a Public Health Notification and Additional Patient Information informing people that the insertion of transvaginal mesh remains an area of serious concern. This was based on over 1,000 complaints filed with the FDA from 2005 to 2007. The complaints only increased in the coming years.
In 2011, the FDA once again informed the people that serious complications associated with transvaginal mesh are possible. This notification was based on some 3,000 complaints received from 2008 to 2010. The complaints were largely against transvaginal mesh inserted for POP repair. Patients suffered the following conditions:
• Transvaginal mesh erosion through the vagina
• Pain during sexual intercourse
• Urinary problems
• Organ perforation
• Bleeding
• Infection
• Pain
• Emotional problems
• Vaginal shrinkage/scarring
• Neuro-muscular problems
• Recurrent Prolapse
While these conditions were suffered by patients of POP repair, patients of SUI repair, also, suffered serious medical conditions. Out of almost 3,000 complaints received by the FDA from 2008 to 2010, over 1,300 complaints were of SUI repair and over 1,500 complaints were of POP repair.
In order to better understand the usefulness of transvaginal mesh over traditional non-mesh for POP and SUI repair, the FDA conducted a comprehensive review of the published scientific literature. Its findings were alarming; the transvaginal mesh for POP repair was no better than the traditional non-mesh product. The FDA has yet to publish its findings on the insertion of transvaginal mesh for SUI repair.
All in all, the FDA found that the insertion of transvaginal mesh did not improve the quality of life of a POP repair patient.
Know Your Rights If You Have Been Wronged
Have you or someone you know had transvaginal mesh insertion and now suffer from its side effects? Was the mesh made by:
• Johnson & Johnson, Inc
• Boston Scientific
• C.R. Bard, Inc
• American Medical Systems, Inc
The Transvaginal Mesh products manufactured by these companies have often been the source of litigation. You may deserve compensation for your pain and suffering.
What you need to know is that the transvaginal mesh was originally manufactured for hernia repair. They were never clinically tested of their usefulness for POP and SUI repair patients, thus the dangerous and painful side effects as mentioned above.
Patients have been subjected to several surgeries to surgically remove the mesh. In some cases, even the surgical removal of the mesh may not be possible, prolonging patient's pain, suffering and not to mention the ever increasing medical bill. To date, over 15,000 transvaginal mesh lawsuits have been filed.
If you have suffered due to transvaginal mesh insertion for either POP or SUI repair, contact transvaginal mesh attorney. They may be able to help you file a lawsuit and make a claim for the compensation that may be needed for meeting the cost of treatment and revision surgery.
To request for more information related to your case, please fill out the form provided on this page.
Q:What will a transvaginal mesh attorney do after assessing my case?
A:A transvaginal mesh attorney is basically a legal expert who will represent you in court and manage your case. He or she will carefully examine your case and determine the right legal path to pursue. You can search online or contact an attorney that specializes in this field to guide you through the legal process.
Q:Is it advisable to contact a transvaginal mesh law firm, if you have suffered injury during the process?
A:Thousands of reports have been received by US Food and Drug Administration from women who experienced injuries and dangerous complications from having the transvaginal mesh implantation done. If you or your loved one has experienced a similar situation, you must contact a transvaginal mesh law firm and file a lawsuit.
Q:What can be the impact of having a lawsuit filed with the help of a vaginal mesh lawyer?
A:If you contact a vaginal mesh lawyer, you will be able to direct the attention of relevant authorities about the complications and injuries that are taking place due to vaginal meshes. Over 600 women have already filed lawsuits against the vaginal mesh manufacturer Ethicon, so that it halts the sales of surgical meshes.
Q:How much will mesh lawyers charge me if I file a case?
A:The legal costs will vary from lawyer to lawyer, and will depend upon many other factors. However, it is still recommended that you seek legal help in your case. A qualified attorney will assess your case and determine your chance at receiving legal compensation. You can also consider class action lawsuits to help lower legal expenses.