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  2. Pelvic Mesh MDL Leadership Defends Settlement Record as ...

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  3. Johnson & Johnsons settles West Virginia pelvic mesh lawsuit

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    West Virginia has reached a $3.9 million settlement with Johnson & Johnson in a lawsuit over the company's marketing of a surgical mesh used to treat pelvic conditions in women, state Attorney ...

  4. Pelvic organ prolapse - Wikipedia

    en.wikipedia.org/wiki/Pelvic_organ_prolapse

    Transvaginal mesh (TVM) has a greater risk of bladder injury and of needing repeat surgery for stress urinary incontinence or mesh exposure. [17] The use of a TVM in treating vaginal prolapses is associated with severe side effects including organ perforation, infection, and pain. Safety and efficacy of many newer meshes is unknown. [16]

  5. Transvaginal mesh - Wikipedia

    en.wikipedia.org/wiki/Transvaginal_mesh

    Transvaginal mesh, also known as vaginal mesh implant, is a net-like surgical tool that is used to treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI) among female patients. The surgical mesh is placed transvaginally to reconstruct weakened pelvic muscle walls and to support the urethra or bladder.

  6. Read the Chart: Law Firms That Got Common Benefit Fees ... - AOL

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  7. Vaginal vault - Wikipedia

    en.wikipedia.org/wiki/Vaginal_vault

    However, the use of a transvaginal mesh in treating vaginal prolapses is associated with side effects including pain, infection, and organ perforation. According to the FDA, serious complications are "not rare." A number of class action lawsuits have been filed and settled against several manufacturers of TVM devices.

  8. Johnson & Johnson Reaches $300M Settlement In Australian ...

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    Johnson & Johnson (NYSE: JNJ) has reached a A$300 million settlement in two Australian class action suits filed by Shine Lawyers for selling defective pelvic mesh implants to Australian women. The ...

  9. Stress incontinence - Wikipedia

    en.wikipedia.org/wiki/Stress_incontinence

    Initially, the FDA approved implantable mesh devices due to their similarity to earlier prototypes, known as the 510(k) process. [ 16 ] [ 17 ] As patients allege long-term harm and suffering as a result of implanted mesh; the FDA released a safety communication in 2008, and led to the reclassification of surgical mesh to a class 3 or high risk ...