Transvaginal Mesh Injury
Transvaginal Mesh Injury Lawyer Yuma
Patients outfitted with medical devices or who've undergone necessary surgery often endure medical care with the belief that their health will improve. The idea that products that are approved for sale and prescriptions are safe give patients peace of mind that they will be taken care of and their health will actually improve with medical device or product intervention. In contrast, not all pharmaceutical and medical device companies have the best interest of patients in mind. On the other hand, profit can become more important than adequate warnings and the provision of information patients need to make informed decisions about their care.
What is Transvaginal Mesh?
A medical device, transvaginal mesh is inserted into the body through the vaginal opening during pelvic surgery, proving reinforcement for conditions including: Pelvic Organ Prolapse and Stress Urinary Incontinence.
Despite the proposed purpose behind transvaginal mesh, in 2011, the Food and Drug Administration warned doctors and consumers alike about the serious risks associated with the surgical mesh. In contrast with other options for treatment and surgery, transvaginal mesh had greater risks, the Administration noted.
Awards & Recognition
AWARDED TO JOHN C. (JACK) ZINDA BY THE NATIONAL TRIAL LAWYERS ASSOCIATION (2016-2020)
AWARDED TO JOHN C. (JACK) ZINDA BY THE NATIONAL TRIAL LAWYERS ASSOCIATION (2017-2020)
AWARDED TO JOHN C. (JACK) ZINDA (2016-2020), JOE CAPUTO (2016 – 2020) & BURGESS WILLIAMS (2016-2017) BY THE NATIONAL TRIAL LAWYERS ASSOCIATION
LIFETIME MEMBERS JOHN C. (JACK) ZINDA, JOE CAPUTO, BURGESS WILLIAMS, NEIL SOLOMON, & JASON ALDRIDGE
AWARDED TO JOHN C. (JACK) ZINDA (2009, 2011-2012, 2014-2021), JOE CAPUTO (2019-2021), BURGESS WILLIAMS (2019-2020), NEIL SOLOMON (2020-2021), & CHRISTINA HAGEN (2021) BY SUPER LAWYERS (A THOMPSON REUTERS COMPANY)
MEMBERS JOHN C. (JACK) ZINDA (2017-2020), JOE CAPUTO (2019-2020), BURGESS WILLIAMS (2019-2020), NEIL SOLOMON (2019-2020), COLE GUMM (2019-2020), CHRISTINA HAGEN (2020) & BRENDAN MCQUAID (2020)
LIFETIME MEMBERS JOHN C. (JACK) ZINDA & JOE CAPUTO
AWARDED TO ZINDA LAW GROUP (2016-2019) BY THE AMERICAN INSTITUTE OF PERSONAL INJURY ATTORNEYS
AWARDED TO JOHN C. (JACK) ZINDA IN 2015, 2016, 2017, AND 2020
AWARDED TO JOE CAPUTO (2016-2019) BY THE AMERICAN INSTITUTE OF PERSONAL INJURY ATTORNEYS
AWARDED TO ZINDA LAW GROUP IN 2018 BY INC.
Awarded to John C (Jack) Zinda (2021) by the American Association for Justice
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Complications and Symptoms of Transvaginal Mesh
While there are some side effects for transvaginal mesh that occur on a more frequent basis, other symptoms and problems may take place less frequently but may have detrimental repercussions. Urinary complications, need for more surgeries in the future, pain, infection and erosion are just some of the issues patients have reported as a result of the defective medical device.
Some of the pain and suffering caused by surgical mesh implanted into the vaginal region makes it difficult for women who’ve had the surgery to perform many of the activities they formerly participated in. Walking, working, sex and other physical activates become excruciating, transforming the very lives of victims of the bad device and their families and loved ones.
In addition, multiple, future surgeries may be necessary to correct some of the damage done to a woman’s body as a result of surgical mesh implantation. The hardship associated with medical bills, time away from one’s career and the difficulties placed on loved ones can produce financial difficulties that may have been unforeseen.
As early as 2011, transvaginal mesh was linked to serious complications and painful side effects. But despite the information and data revealed, some women and doctors were not adequately warned about the risks associated. In the same year, the Food and Drug Administration recognized the side effects and possible dangers tied to the use of transvaginal mesh used for Pelvic Organ Prolapse and Stress Urinary Incontinence. More than 3,500 reports of negative, sometimes serious, side effects were reported to the FDA by 2011, highlighting the serious flaws of the medical device.