Tag: medical recall
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.
Start your Oculentis claim today
If you’ve yet to start your Oculentis claim, here’s some information about getting started today. It’s important to claim as soon as you can.
If you’re one of the hundreds of people who have suffered with opacification problems having been fitted with intraocular lenses manufactured by Oculentis, you may have a claim for compensation. The blind spots and cloudiness in the vision can be caused by calcification from phosphate that was previously used in the manufacturing process.
The way to correct the problem is to have further surgery for the lenses to be replaced. You may be able to claim personal injury compensation for having to undergo the further surgical procedure.
Compensation action for victims of the Oculentis recall
If you’ve been affected by the Oculentis recall, you may be eligible to join our compensation action with No Win, No Fee representation.
If you’re one of the hundreds of people who have been affected by the opacification problems related to surgically-implanted intraocular lenses, we may be able to help you. If you’ve been suffering with blind spots ore cloudiness in your vision, and needed / need corrective surgery, you could be entitled to thousands of pounds in compensation.
Even if you didn’t have to pay for the revision surgery, you could still be eligible to make a claim. But hurry: time limits for these types of cases can lead to people missing out on their chance to make a claim.
Oculentis compensation action
If you’ve yet to initiate your legal action for Oculentis compensation, make sure you speak to our team as soon as you possibly can.
In this type of action, there can be complicated (and multiple) time limits to claim. Missing one or more of these deadlines could mean the difference between receiving thousands of pounds in compensation or getting absolutely nothing at all.
You may be eligible to claim Oculentis compensation if you’re one of the hundreds of people affected by the recall of their intraocular lenses.
Valsartan recall widens
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 recall?
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.
Bone cement complications from product recall
A regulator warning earlier this year stemmed from bone cement complications caused by an issue with the product itself.
A risk of the need for revision surgery from the use of Optipac 40 Refobacin Revision and Optipac 80 Refobacin Revision was identified. Manufacturer, Biomet UK Limited, issued a Field Safety Notice at the end of last year. The UK’s medical regulator, the MHRA (Medicines and Healthcare products Regulatory Agency), issued their own recall advice off the back of the findings.
Anyone who has suffered with bone cement complications may find the reason is to do with the product itself as opposed to failed surgery.