Helpful Information
Bringing a hip replacement claim
If you have suffered ongoing pain or injury following hip replacement surgery, there are multiple scenarios where you may have a strong basis to bring a compensation claim. This includes the following:
- The implant used in your surgery has a known design flaw – models by certain brands have been known to cause premature failure, loosening, or metallosis.
- Poor surgical technique was applied during your surgery – If the surgeon improperly positioned or installed the implant, leading to complications, you may have the basis to bring a claim.
- Inadequate post-surgical care given – If post-operative care was negligent, resulting in infection or other complications, you may be entitled to compensation.
- Failure by the healthcare provider to warn of the risks – If you were not adequately informed of the risks associated with the implant, there may be scope to bring legal proceedings.
- The device featured a manufacturing defect – You may have a claim if the implant had a manufacturing defect that led to failure.
- An incorrect type of implant was used – If the wrong type or size of implant was used, causing you pain and suffering, you are likely to have a basis to bring a claim.
To prove your case, it’s necessary to demonstrate that the device manufacturer or the healthcare provider owed a duty of care, breached that duty through actions or omissions, and directly caused harm or injury as a result. Evidence such as medical records, expert testimony, and documentation of the injury’s impact are crucial in establishing this breach and the causal link between the negligence and the resulting harm. Proving negligence requires clearly linking the provider’s actions to the your adverse outcomes.
Our experienced medical negligence team will help you gather the necessary evidence and build a strong case to hold the responsible parties accountable. Arrange a time to speak with a solicitor here by completing our confidential online form.
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Meet John McCarthy
John McCarthy is a partner at McCarthy + Co Solicitors LLP, with more than 20 years of experience in medical negligence and product liability claims, including defective hip replacement cases involving metallosis, implant loosening, and premature failure. He brought multiple successful claims against DePuy Orthopaedics following the worldwide recall of the ASR hip replacement system and continues to act for clients fitted with hip implants from manufacturers such as DePuy, Stryker, and Zimmer Biomet.
John holds a diploma in civil litigation from the Law Society of Ireland and is a member of Action Against Medical Accidents (AvMA), the leading patient safety charity. He is also the author of A Patient’s Guide to Bringing a Claim for Medical Negligence. If you have been fitted with a defective hip replacement, you can contact John directly at john@mccarthy.ie.
Frequently Asked Questions
Some of the questions often posed to our medical negligence team.
Which hip implant brands have been known to fail?
Several hip replacement implant brands have been associated with high failure rates, including DePuy Orthopaedics’ ASR and Pinnacle metal-on-metal systems, which were recalled due to issues like metallosis and implant loosening. Stryker’s Rejuvenate and ABG II models were also recalled for similar problems, including corrosion and fretting, leading to tissue damage and implant failure. Zimmer Biomet’s Durom Acetabular Component faced issues with loosening and poor fixation. Wright Medical’s CONSERVE and Profemur implants have also been linked to premature failure and complications.
What laws govern the use of hip replacement devices?
In Ireland, the regulation of medical devices is overseen by the Health Products Regulatory Authority (HPRA), which enforces both EU and Irish laws to ensure the safety and quality of these products. The EU Medical Device Regulation (MDR) 2017/745 establishes stringent standards for the safety, performance, and quality of medical devices across the European Union. In Ireland, these standards are implemented through the Medical Devices Regulations (S.I. No. 252/2021), which transposes the MDR into national law and outlines the obligations of manufacturers, importers, and distributors of medical devices.
What are the time limits for bringing a claim in Ireland?
The time limit for bringing a claim is generally two years from the date you became aware of the injury or the defect in the implant. This is known as the “date of knowledge.” If the injury or defect is not immediately apparent, the two-year period begins when you first discovered or should have reasonably discovered the problem. In cases involving medical negligence, the same two-year limit applies. It’s important to seek legal advice promptly to ensure your claim is filed within this statutory period.
Is a solicitor necessary to bring a claim?
While it is not legally required to have a solicitor to bring a claim, it is highly advisable. A solicitor can navigate complex legal procedures, gather essential evidence, and negotiate with insurers or opposing parties on your behalf. They ensure that your claim is filed correctly and within the legal time limits, significantly increasing your chances of a successful outcome. Without a solicitor, you may struggle with legal technicalities and miss critical deadlines, potentially weakening your case or resulting in a lower settlement. A solicitor’s expertise is invaluable in maximising your compensation.
Useful resources
Some links relating to this topic that you may find useful.
- Drugwatch – Hip Replacement Lawsuits
- ConsumerNotice.org – Hip Replacement Lawsuits
- OrthoInfo – Total Hip Replacement
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