Patients across Limerick, Clare, Tipperary, Kerry, and Cork are being urged to review their medical records following a product recall issued by Zimmer Biomet. The recall relates to the NexGen Complete Knee Solution, a widely used knee replacement device implanted in patients across the North Munster region, including many who attended Croom Orthopaedic Hospital.
Background to the Recall
Zimmer Biomet issued a recall notice concerning specific lots of its NexGen implant components. These devices were implanted primarily around 2015 and 2016. The company’s letter, issued to surgeons and healthcare providers, highlights concerns over aseptic loosening, a condition where the knee implant can detach from the bone without infection, potentially leading to pain, reduced mobility, or the need for revision surgery.
🔗 View the official recall letter here (PDF)
Patients May Be Unaware
Despite the recall being issued in 2022, it appears that not all affected patients have been informed. Some recipients only received letters in 2023, while others may still be unaware that the device used in their surgery is included in the recall.
There is also concern that many patients have not been advised to undergo revision surgery, even though their implants are potentially affected.
Legal Implications for Patients
Patients who received the recalled implants may have grounds for a product liability claim, particularly if they have suffered pain, required additional surgery, or were not adequately informed of the recall.
However, the Statute of Limitations could be a barrier in some cases. In Ireland, patients generally have two years from the “date of knowledge” of the injury or issue to initiate legal action. Since some recall letters were only received in 2023, affected individuals may still have time to explore their legal options.
How Crimmins Howard Can Help
If you had a knee replacement around 2015 or 2016 and attended Croom Orthopaedic Hospital or any other hospital in the Munster area, it may be worth investigating whether your implant was part of the Zimmer Biomet recall.
Our experienced medical negligence and product liability team can:
- Help determine whether your implant is affected
- Advise on your legal rights
- Assist in pursuing compensation if the device has caused harm or required revision surgery
Contact us today for a confidential discussion. Early legal advice is crucial to protect your rights.
