Scottish Mesh Survivors’ Transvaginal Mesh Petition
In June 2014, a Scottish advocacy group known as Scottish Mesh Survivors presented a transvaginal mesh petition, PE157, for a safety review of transvaginal mesh implants before a hearing of the Scottish government’s Public Petitions Committee. According to the BBC, Scottish Mesh Survivors is comprised of women and healthcare professionals who have used transvaginal mesh devices. During the transvaginal mesh petition hearing, members of the group requested that the government prohibit transvaginal mesh implantation procedures in order to conduct a review of the safety and efficacy of these devices.
If you or someone you love has been fitted with a transvaginal mesh implant and you suffered from adverse side effects or life-threatening complications, you may be entitled to recover damages for your injuries. Contact us today to learn more about your legal options and pursuing a claim for compensation.
What is the Transvaginal Mesh Petition?
In January 2012, several transvaginal mesh manufacturers such as C.R. Bard and Johnson & Johnson were ordered by the U.S. Food and Drug Administration (FDA) to begin three-year studies to examine the safety of their products. Other countries are now considering requiring additional clinical trials for the same purpose.
During the Public Petitions Committee hearing in Scotland, for instance, one of the members of Scottish Mesh Survivors shared the group’s initiative to create a safety information booklet in which the group plans to include known complications and risks associated with transvaginal mesh implants. According to the member, she was unaware of potential dangers of transvaginal mesh prior to receiving the device. In addition to proposing a transvaginal mesh petition requesting further review of the products, Scottish Mesh Survivors claim that that their use of transvaginal mesh implants resulted in severe health complications that completely altered their lives. For some women, the implant allegedly transformed from pliable and soft to inflexible and heart, thus resulting in internal injuries.
Transvaginal Mesh Overview
Women who have had repeated pregnancies or childbirths or those who are of menopausal age may be suffering from a weakened pelvic floor. As a result, these individuals may develop stress urinary continence or pelvic organ prolapse, a condition in which the woman’s rectum, uterus or bladder may sink into her vagina or protrude from her body. To help to support the pelvic, transvaginal mesh implants are fitted into women by way of a surgical procedure. While there is little question about the success of transvaginal mesh implants, it is the devices themselves that are raising concerns among the public and medical communities across the world. According to patients, transvaginal mesh devices may cause problems, including:
- Vaginal scarring
- Mesh erosion
- Inability to sit
- Pain during sexual intercourse
- Urinary problems
- Bowel, bladder and blood vessel perforation
As a result, women may consider filing lawsuits against the manufacturers to seek compensation for their injuries. Medical device companies such as American Medical Systems, Coloplast, Johnson & Johnson, Boston Scientific, C.R. Bard, Gynecare/Ethicon, and Cook Medical have all been named as defendants in pending lawsuits.
Have You Been Injured? Contact Transvaginal Mesh Attonrey
If you or a loved one was fitted with a transvaginal mesh implant or if you have questions about the Scottish transvaginal mesh petition, contact us today. There is no cost to speak with us, and we can help you to determine if you are entitled to seek compensation for your injuries. We can also place you in contact with an affiliated attorney who can assist you in recovering the damages to which you may be entitled.