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.
The vaginal mesh scandal has hit the news again this week as we continue to represent victims claiming compensation for pelvic mesh procedures that have gone wrong.
The invasive surgical procedure was under a widespread pause last year following further reviews into the safety and efficacy of the devices. In April this year, revised guidelines were released by NICE (The National Institute for Health and Care Excellence), which many have argued do not go far enough.
We know from years of experience and from the clients that we help that the impact of mesh gone wrong can be absolutely awful.
A medical device alert has been issued and published by the MHRA in relation to Ethicon surgical staplers, which have reportedly caused injury to some patients.
It’s understood that there’s a risk that some of the devices manufactured from March 2018 have not been working properly. Reported issues include the devices misfiring or failing to fire the staples during surgery. The MHRA (Medicines and Healthcare products Regulatory Agency) say that there has been increased complaints of malformed stables with some devices being returned.
With this issue involving invasive surgery, the alert is one that needs to be taken incredibly seriously.
If you’re suffering with elbow implant problems, you may want to read this. The recent Stryker recall could be linked to any complications you’re experiencing.
Back in November 2017, a Field Safety Notice was filed for a recall of the rHead Radial Head and the Uni-Elbow prosthesis. In February this year, a medical device alert was put out by the MHRA (Medicines and Healthcare products Regulatory Agency). Urgent actin is to be taken, and any patient suffering should seek medical advice.
The problems that could be caused that are linked to this recall can be serious. Having recovered over £1.3m in damages for victims of the PIP implant scandal, as well as representing Claimants in hip implant cases and other medical device actions, these kinds of claims are one of our primary specialisms.
We’re taking on claims for those who need to launch a hernia mesh lawsuit UK case. We’re already acting for a number of victims, and anyone who has yet to start their claim is being urged to speak to us as soon as they can.
We can tell you from years of experience that medical product claims can be complicated. In one medical product group action alone, we’ve recovered over £1.3m damages (and counting); so, you know you can trust our advice.
One of the major issues is the limitation periods that can apply to these types of claims. There can be more than one, and plenty of people end up missing deadlines in lawsuits. Missing those deadlines can cost Claimants literally tens of thousands of pounds in unrecoverable compensation. It’s important to act fact!
The Gatwick drone incident that has brought one of the UK’s biggest airports to a complete standstill this week raises big legal questions.
We’ve written before about the use of smart technology and how it can be dangerous. Although the Gatwick drones appear to be high-tech and are being used as part of what appears to be a deliberate ploy, everyday drones can be dangerous. It’s those drones that can be easily bought online or on the high street that raise the legal questions as well.
If something happens, where’s the liability? Where’s the insurance? What do we need to do to ensure people are protected?
The Valsartan recall widened last month following updated advice from the Medicines and Healthcare Regulatory Authority (MHRA).
Batches of products containing Valsartan that were supplied by Teva UK Ltd and Mylan are being recalled in the UK. This follows on from a drug alert earlier this year that was issued after the discovery that some Valsartan products were contaminated. Legal cases are already underway, and this latest recall involves further batches of the product.
An immediate suspension and quarantine of the additional affected products has been ordered.
Were you affected by the cough syrup mould issues that came to light over summer? In the midst of the season for colds and coughs, you may want to take heed of this warning if you’re not aware of it already.
Over summer, a formal recall was issued with the UK’s medicines regulator, the Medicines and Healthcare products Regulatory Agency. This was a Class 2 Medicines recall for own-brand glycerine and blackcurrant cough syrup products manufactured for children by Bell, Sons & Co.
As these are marketed as own-brand products, it’s the likes of Asda, Morrisons, Sainsbury’s and Tesco at the centre of this recall.