
Roszczenia dotyczące wadliwych urządzeń medycznych
Roszczenia z tytułu wadliwych urządzeń medycznych obejmują protezy stawu biodrowego, protezy stawu kolanowego, wadliwe defibrylatory i rozruszniki serca, wadliwe siatki chirurgiczne, implanty piersi PIP itp. Roszczenia mogą powstać, gdy takie urządzenia spadną poniżej akceptowalnego standardu i pojawią się komplikacje dla pacjentów.
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Czym są wadliwe urządzenia medyczne?
Stosowanie wyrobów medycznych stało się stosunkowo powszechne i jest najczęściej wykorzystywane do wymiany stawu biodrowego lub kolanowego, urządzeń monitorujących pracę serca, implantów kosmetycznych i siatek chirurgicznych. Urządzenia medyczne są na ogół rygorystycznie testowane przed użyciem w chirurgii, aby zapewnić ich skuteczność i bezpieczeństwo. Niestety, czasami stosowane urządzenia medyczne spadają poniżej akceptowalnego standardu i powodują komplikacje u pacjentów. Stało się to bardziej widoczne w ostatnich latach, szczególnie biorąc pod uwagę niedawne skandale dotyczące wadliwych siatek chirurgicznych i implantów piersi PIP.
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Metal-On-Metal Hip Replacement Claims – These devices have been shown to fail much earlier than expected and may cause injury due to metal particles released as the implants wear over time. This can have serious consequences, including the need for additional surgery in some cases.
Knee Replacement Claims – Claims are often made due to issues occurring because of the way the knee replacement was fitted, the product being defective, further injury being caused because of the product being fitted incorrectly and knee replacement complications leading to further surgery.
Faulty Defibrillator Claims – The device failing can either result in unnecessary shocks, causing discomfort to the person wearing it, or the failure to provide a lifesaving shock if an irregular heart rhythm develops.
Cochlear Implant Claims – Defective cochlear implants can cause painful sounds and the distress of having more surgery to get the implant replaced. There is no simple fix to a faulty cochlear implant – and in some cases, these problems are the responsibility of the implant manufacturer.
Sorin Stochert 3T Heater – Cooler Claims – Sorin Stockert 3T Heater-Coolers are used to keep patients at the right temperature during heart surgery and other complex surgical procedures. It is believed that some of these devices have become contaminated with Mycobacterium chimaera and that the devices are passing bacterial infections on to patients. The bacterium is very resistant to antibiotics and additional surgery may also be required to replace implants if they have been infected.
Faulty Pacemaker Claims – Pacemakers are a very useful device to help people with heart problems regulate their heartbeat. While most pacemakers work effectively, a manufacturing fault has been identified in some of the devices which means they do not operate effectively. Such issues would likely be the responsibility of the manufacturer.
Poly Implant Prostheses (PIP) – PIP implants are silicone breast implants that contain a defective silicone gel. Approximately 47,000 women across the UK had PIP implants fitted and many have been experiencing complications. While the use of PIP implants has now been banned, many women have been living with the implants and are fearful that they might rupture resulting in serious health problems.
Surgical Mesh Implants – These implants have been used to treat women suffering from Pelvic Organ Prolapse and Stress Urinary Incontinence. The use of surgical mesh has been under intense scrutiny in recent years as hundreds of women have reported serious complications and have made claims for compensation against the manufacturer and the NHS.

Najczęściej zadawane pytania
Najczęściej zadawane pytania
Biorąc pod uwagę poważne konsekwencje leczenia wadliwym wyrobem medycznym, producenci i świadczeniodawcy usług medycznych muszą zapewnić bezpieczeństwo produktów przed ich użyciem u pacjentów. Jeśli tego nie zrobią, a pacjent poniesie straty i szkody, może ubiegać się o odszkodowanie.
Our product liability and medical negligence solicitors in Belfast, Dungannon & Dublin will advise you on the most appropriate course of action. This may involve suing the product manufacturer for creating a defective product or the healthcare provider for failing to fit the device correctly or failing to adequately warn the patient of the potential risks associated with the device. In some cases, it will be necessary to sue both the manufacturer and the healthcare provider as fault may lie with both.
Nasi prawnicy zajmujący się zaniedbaniami medycznymi
P.A. Duffy & Co
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