The increasing number of pelvic mesh implant complications has finally forced the NHS to put a widespread halt on the use of the procedure as more and more women come forward with problems over the use of transvaginal mesh and transvaginal tape.
We’ve been advising women suffering mesh implant complications since the start of 2013, and our Group Action Lawyers are involved in legal action over the use of the devices. We wholeheartedly welcome the NHS pause on the use of the implants that’s arisen from a review chaired by Baroness Julia Cumberlege.
This may prove to be another crucial step forward toward justice for the many women who have suffered catastrophic and lifelong injuries caused by mesh implant complications.
Some pelvic mesh devices were reportedly “rushed to market” without proper testing and warnings for women, the legal team for a Claimant pursuing damages for pelvic mesh injuries claims.
According to the reports, manufacturer C.R. Bard moved pelvic mesh devices to market quickly and failed to properly test the devices and provide sufficient warnings over their use.
The Claimant alleges that the ‘Avaulta Solo Support System’ and the ‘Align Trans-Obturator Urethral Support System’ are unsafe, and inadequate warnings were provided to her. She has reportedly suffered debilitating injuries.
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Our legal team have been assisting people in various situations involving harm caused by vaginal mesh implants.
The UK government review update is welcome news.
Years after the UK’s Medicines & Healthcare products Regulatory Agency (MHRA) investigated issues and decided against recalls and bans, the National Institute for Health and Clinical Excellence (NICE) has suggested the surgery should be banned, and New Zealand have become the first country in the world to put an outright ban in place.
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The infamous mesh implants that’s sewn into vagina walls which has reportedly caused multiple injuries and excruciating pain for many women may now be finally banned for good in the U.K.
Those women who had the ‘minor’ routine surgery to help treat organ prolapses and mild incontinence, but then went on to suffer serious and painful complications has prompted the U.K.’s National Institute for Health and Care Excellence (NICE) to recommend that the implants shouldn’t be used in treatment any more at all, only for research.
This is a change to previous NICE guidelines that were more about taking extreme precautions when using the mesh devices.
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A federal court has dismissed Boston Scientific’s appeal against a £20 million settlement sum awarded to four claimants who sued the company for alleged defective pelvic mesh implants.
The claimants argued that the Pinnacle mesh used to treat pelvic organ prolapse and female stress urinary incontinence was defective and caused significant pain and injuries.
Pain, bleeding and infection are potentially commonplace if the devices fail and the plastic mesh fuses and cuts in to the patient. As they cannot usually remove the mesh from the vaginal walls, the outcome for those whose devices fail can be lifelong and serious.
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