Category: Recalls
Stanmore hip implant recall
The Stanmore hip implant recall published earlier this year relates to the potential for some Modular Femoral Heads being contained in the incorrect packaging.
The urgent Field Safety Notice issued by Stanmore Implants – who are a part of the Stryker Corporation – outlines the issue and the potential dangers. It may be that patients could be fitted with the incorrect implant heads if the problem is not identified by surgeons and medical staff at the time of an operation.
As with most medical implant problems, this recall is a serious matter, and we have seen the damage that can be done to patients when things go wrong with hip implants.
Ethicon surgical staplers medical device alert
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.
Legal advice for TVT surgery claims
Following the criticism over the new guidelines that came out last month, we’ve received further enquiries from people asking for advice about TVT surgery claims.
With the issues surrounding vaginal mesh in the news again, here’s some advice for you if you’ve yet to speak to anyone about your options for compensation.
One of the first things we often remind people about is to make sure that you seek advice as soon as you can. There can be a number of timeframes to start a case in a legal action of this nature. Leaving it too late can be the difference between receiving tens of thousands of pounds or getting absolutely nothing as a victim of TVT surgery gone wrong.
Raindrop near vision inlay recall
The Raindrop Near Vision Inlay recall has been initiated due to an increased risk of corneal haze that patients implanted with the devices may experience.
A Medical Device Alert was issued via the MHRA (Medicines and Healthcare products Regulatory Agency) a few weeks ago. There’s a warning to not implant Raindrop Near Vision Inlays and to dispose of any unused stock of them.
Any patients who have already been implanted with the inlays are to be monitored, and any incidents and problems are to be reported. This recall follows the recent news coverage about the Oculentis recall, which is one of the compensation actions we’re representing people for.
Concerns raised over new vaginal mesh guidelines
Following last year’s widespread pause, the new vaginal mesh guidelines have been published. Understandably, concerns have been raised that they may not good enough.
We can tell you from experience that the complications and suffering that women can endure when vaginal mesh surgery goes wrong can be horrendous. We’re acting for women on a No Win, No Fee basis who are making claims for personal injury compensation because of problems they’ve experienced. With some women left unable to work or walk ever again, the continued use of these devices must be heavily scrutinised.
Concerns have been raised that the new vaginal mesh guidelines that have been published haven’t considered the experiences of the victims, and don’t go far enough to protect women who may undergo the procedure.
Elbow implant problems and Stryker recall
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.
Are you suffering with valsartan side effects?
If you’re suffering with valsartan side effects, you may want to read this article and take heed of some important information about the drug.
Last year, a Class 1 Medicines Recall was initiated by Medicines and Healthcare products Regulatory Agency (MHRA). The recall stems from potential contamination that comes from the production process that could be incredibly serious for anyone affected. In fact, in the US, lawsuits have been active for some time now. When members of the Group Action Lawyers attended a conference in the U.S. last year, it was clear to us just how serious this issue could be.
If you’ve been taking the medication here in the UK and you’ve suffered problems or side effects, we may need to speak with you.
Are you affected by the bard mesh recall?
If you’re affected by the Bard mesh recall, is there any immediate danger, or is there any action that you need to take?
We can’t say that we’re surprised by the news of the recall. We’ve been advising women for years who have suffered problems and complications that have stemmed from being fitted with a vaginal mesh device. We’re also representing women who are making mesh implant compensation claims.
The company has initiated a recall and has immediately ceased production and distribution in Europe as a result of not wanting to invest further resources in evolving regulations. So, what does this mean for the patients?
Yet to start your transvaginal mesh claim? Read this now!
If you’ve yet to start your transvaginal mesh claim for compensation, we recommend that you read this urgent advice about your options for justice.
We know that people put off starting a legal case for many reasons. One of the main ones is the worry about having a formal legal claim. But if you leave it too late, you risk being unable to claim at all.
There can be a number of timeframes involved in a case like this, and we’ve had to turn people away in the past who have missed deadlines to claim. We don’t want you to miss out on your chance for justice. With that in mind, here’s a little useful guidance about making a transvaginal mesh claim for compensation.
Starting your vaginal mesh lawsuit with us
Starting your vaginal mesh lawsuit with the Group Action Lawyers, if you’ve yet to do so, can be quick and easy.
In the UK, there has been legal actions going on for quite some time. However, it’s taken a while for regulators and the NHS to really act on vaginal mesh complications that people are suffering from. Only last year did the NHS finally put a widespread pause on the use of mesh implants, pending further investigations. Although there are still few definitive answers we need in terms of the problems people are suffering from, we’re taking legal action for women who are suffering with problems.
We’re calling on anyone who has yet to initiate a vaginal mesh lawsuit in the UK to contact our team as soon as possible.