As supported by the July 2011 U.S. Food and Drug Administration (FDA) warning, transvaginal surgical mesh implants used to repair pelvic organ prolapse (POP) have unnecessarily exposed thousands of women to significant and undisclosed risks of serious injury. Most of these transvaginal mesh side effects can lead to severe and emergency situations, requiring:
In many cases, the mesh cannot be completely removed, and it, therefore, permanently compromises the health of the woman affected. If you needed further treatment because an implant used to treat your POP failed and caused you unnecessary pain and suffering, talk with our seasoned transvaginal mesh implants lawsuit lawyers today.
Our attorneys understand that not only do the women affected experience extreme pain, but entire families suffer as well. Women affected by transvaginal mesh may no longer be able to work or bring the same level of income as before, and they may be prevented from providing necessary household support due to their injuries.
The FDA voiced their concern in a warning issued on July 13, 2011, that the device does not provide the best solution to POP or Stress Urinary Incontinence.
“There are clear risks associated with the transvaginal placement of mesh to treat POP,” said William Maisel, M.D., M.P.H., deputy director and chief scientist of the Center for Devices and Radiological Health. “The FDA is asking surgeons to carefully consider all other treatment options and to make sure that their patients are fully informed of potential complications from surgical mesh. Mesh is a permanent implant—complete removal may not be possible and may not result in complete resolution of complications.”
If the walls of the vagina weaken after childbirth, internal support for many of the pelvic organs, including the bladder, rectum, or uterus, may be eliminated. Without this support, the organs can prolapse, or “drop,” causing women both discomfort and pain.
A prolapse of these organs can happen after a woman undergoes a hysterectomy because the removal of the uterus can also lead to a lack of support for the pelvic organs. Transvaginal mesh implants were created as a way to permanently provide extra support to these organs. The implants are also used to treat Stress Urinary Incontinence.
Although the FDA is now asking medical professionals to advise patients about these dangerous implants, there are women whose lives have been severely impacted prior to this warning and without knowledge of the hazards to their health. Our firm has been heavily involved in this litigation regarding transvaginal mesh implants and other defective medical devices.
We are knowledgeable and aggressive in gaining the compensation owed to victims who have been affected by defective products and corporate negligence. Talk with our transvaginal mesh attorneys today about the injuries you have sustained by calling our firm now.
Michelle is a founding partner of Zoll & Kranz, located in Toledo, Ohio. Michelle has been a plaintiff’s lawyer for the entirety of her practice – over 32 years. She devotes the majority of her time to complex consolidated litigation and class action including advocating for people injured by medical devices, prescription medications, or corporate negligence.
This article has been written and reviewed for legal accuracy and clarity by the team of writers and attorneys at Zoll & Kranz, LLC and is as accurate as possible. This content should not be taken as legal advice from an attorney. If you would like to learn more about our owner and experienced Ohio injury lawyer, Michelle L. Kranz, you can do so here.
Zoll & Kranz, LLC does everything possible to make sure the information in this article is up to date and accurate. If you need specific legal advice about your case, contact us. This article should not be taken as advice from an attorney.
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