Penningtons Manches Cooper investigates M6-C artificial cervical disc device failure
Recent reports regarding the M6-C artificial cervical disc, including regulatory recall action by the UK Medicines and Healthcare products Regulatory Agency (MHRA), have raised concerns for patients who have undergone cervical disc replacement surgery using this device.
Penningtons Manches Cooper is currently investigating potential legal claims on behalf of individuals who have received an M6-C implant and may have experienced complications or have been affected by the recall. Concerns may include device failure, premature wear, inflammation, pain, or the need for revision surgery.
If you have been implanted with an M6-C artificial cervical disc, it is important to seek medical advice so that you can be actively monitored and understand potential treatment options available to you. Even if you are not currently experiencing symptoms, you may have questions about future risks or next steps following the recall.
How we can help
The specialist medical negligence team at Penningtons Manches Cooper is currently investigating claims on behalf of individuals affected by the device and can provide clear, practical guidance tailored to your circumstances.
Get in touch
If you have an M6-C implant and would like to discuss your situation, please contact us in confidence. We can assess your case and advise you further in relation to a potential negligence claim. Seeking advice as early as possible can help ensure your rights are protected.
Contact
Lyndsey Skibinski by email or call her on 020 7457 3008. Alternatively, complete our online enquiry form and a member of our team will be in touch.