
As stories of vaginal mesh complications continue to emerge, many of those who have suffered from the implants are seeking treatment to lessen or stop the pain and injuries they have faced. However, the difficulties of vaginal mesh removal can mean that some of the harmful consequences are, unfortunately, irreversible.
Vaginal mesh implants, used to treat things like urinary incontinence and pelvic organ prolapse, have been the subject of controversy for many years. While approved by the UK regulator, the MHRA, the issue of serious complications can be shocking, with many women speaking out about the complications that they have suffered. In response, we have taken on claims from many women affected by the implants, who we believe are eligible to claim compensation for the harm they have been caused.

In a huge win for anyone harmed by medicines or medical devices, the government has agreed to the appointment of an Independent Patients’ Commissioner. Their role will be to stand up for people who have fallen victim to the dangerous side-effects of certain medical products.
At The Group Action Lawyers, we have been raising the unheard voices of suffering patients for many years, taking on many clients in large group and multi-party actions against powerful medical companies and manufacturers. As such, we welcome the news of this new public service, which represents a significant step in the right direction for patients and overall safety.

If you have suffered as a result of complications arising from the use of Essure, perhaps leading to the removal of the device or a recommendation by your doctor to have Essure removed, you could be one of the many eligible to make Essure compensation claims with the Group Action Lawyers.
Essure is a form of permanent birth control that is usually fitted whilst a patient is awake. It is then designed to sterilise the recipient and was manufactured by Bayer HealthCare in the United States but has been fitted in women across the globe.

In some cases, the chance of hernia complications occurring post-op is up to 30%. A U.S. study reportedly indicates that hernia complications are most likely to occur at least 30 days after surgery.
The study looked into all incisional hernia repair hospital admissions between 2010 and 2014 and found that, out of almost 16,000 patients, almost 20% were readmitted within one year of their surgery, and 60% of were readmitted after 30 days. Of the 16,000 patients, 88% were reportedly treated using hernia mesh, and one-third had to undergo further major surgery.
This extremely high percentage of both short-term and long-term readmissions could indicate how dangerous the use of hernia mesh can be. The complications arising from hernia mesh over 30 days after surgery can be incredibly serious. In the UK, the MHRA (Medicines and Healthcare products Regulatory Agency) has been criticised for failing to review the use after patients came forward with complications. As a law firm, we represent people claiming compensation for hernia mesh problems.

The Group Action Lawyers fight for justice in a number of emissions compensation actions, representing clients for claims on a No Win, No Fee basis.
This includes cases against Mercedes, Porsche, and Nissan and Renault. If you have been a part of a recall for any of those carmakers, we may be able to take a compensation case forward for you now.
Here is a little advice about our emissions work and our experience in this area of law. To get in touch with the team now, please see our Contact Page here.

We represent victims for hernia mesh compensation claims and we can work for our clients on a No Win, No Fee basis, with a free initial case assessment.
We understand how severe the pain and problems can be when hernia mesh has gone wrong. Claiming compensation can be important for any victim to receive some form of justice for what they have to go through.
Here is some guidance about when you could claim, what you could claim for, and how we assess claims to bring them to a successful conclusion.

The results of the recently published report that follows a large-scale pelvic mesh inquiry raises significant concerns about how women have been treated over this issue.
As the legal representatives for a number of women claiming compensation, the report results did not come as much of a surprise to us. That being said, it was no less worrying to see the results of it.
For some, it may act as some form of vindication. Either way, we represent victims for compensation cases, and if you have yet to look into making a claim, we urge you to speak to our team as soon as you possibly can to avoid missing out.

News of the Johnson & Johnson pelvic mesh settlements in Scotland are welcome here at the Group Action Lawyers as the wider fight for justice continues.
Settlements have now been achieved for thousands of people worldwide, and millions of pounds in damages have been paid out. But the battle for many women rages on, and we represent people for cases here in England and Wales.
Here, we will briefly cover the settlement in Scotland and how this affects vaginal mesh claimants in the rest of the UK.

If you need to make a pelvic mesh compensation claim, we may be able to represent you for a legal case on a No Win, No Fee basis.
We already represent several women suffering from horrendous problems and complications that arise from vaginal mesh issues, and we may be able to help you too. We often warn that women who think they may have a case should contact us as soon as they can to avoid missing any deadlines to claim. In cases like this, there can be numerous deadlines and you do not want to miss any.
We recently wrote an article about deadlines which you can also read here. For more information about making a claim for vaginal mesh injuries, read on.

Patient information leaflet errors can, in the worst-case scenarios, cause severe problems for those who have used the wrong medication or used meds incorrectly due to the error.
When these scenarios happen, a recall will usually be launched and announced via the Medicines and Healthcare products Regulatory Agency (MHRA). Information about the recall will normally be distributed so that patients can be made aware, but this won’t always stop an adverse incident from occurring.
With this in mind, here’s a little advice about what to do if you have suffered harm as a result of following the incorrect information for medication or a product in general.