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Exactech Hip Replacement Lawsuits

NYC Defective Device Lawyers

Patients who have undergone hip replacement surgery and received the Exactech Connexion GXL Acetabular Liner have reported significant issues, including early device failure, often within the first year after implantation. For those who trusted this device to restore mobility and reduce pain, the resulting complications—such as discomfort, limited mobility, or joint instability—can be devastating, especially when facing the need for a second surgery.

At Rheingold Giuffra Ruffo Plotkin & Hellman LLP, we understand the distress and frustration caused by defective hip implants. Our team of experienced attorneys has decades of experience holding medical device manufacturers accountable for the harm caused by their products.

If you or a loved one is suffering due to a failed hip implant, contact us online or call (212) 684-1880 for a consultation.

Evidence of Hip Implant Failure

According to reports from Drug Watch, the Exactech Connexion GXL Acetabular Liner is made from polyethylene and is marketed as a durable solution for hip replacement patients. Despite these claims, many patients have experienced early failure of the device. The polyethylene material can degrade, leading to the buildup of debris within the joint, causing tissue damage, bone loss (osteolysis), and ultimately, loosening of the implant. These complications often result in the need for painful revision surgery.

Medical studies published in The Journal of Arthroplasty and Arthroplasty Today have documented the premature wear of the Exactech Connexion GXL Acetabular Liner. Orthopedic surgeons have observed rapid deterioration of these liners in their patients, leading to significant bone erosion and implant failure. These findings have prompted surgeons to inform affected patients that revision surgery may be necessary due to the excessive wear and loosening of the implant.

Moreover, the FDA’s MAUDE database has recorded numerous adverse event reports related to the Exactech Connexion GXL acetabular liners, with many citing the early wear of the liner. Studies have also shown that cross-linked polyethylene, used in the Connexion GXL liner, is more prone to fatigue damage compared to conventional polyethylene, especially when placed at certain angles during surgery.

Exactech’s Surgeon Notification

In June 2021, Exactech issued a warning letter to orthopedic surgeons about the early failure rates of their hip replacement devices. They advised surgeons to contact patients who had received the device within the last six years for a medical evaluation to determine if the hip implant was showing signs of failure. It is estimated that nearly 90,000 patients may be affected by this defect.

If you suspect that your Exactech hip implant may be failing, it is critical to consult your surgeon. Our firm has extensive experience in handling defective hip implant cases and can help you navigate the legal process to seek compensation for your injuries.

Symptoms of Hip Implant Failure and the Importance of X-Rays

Exactech’s recall notice advises patients to undergo X-rays every two years, even if no symptoms are present, to monitor for potential device failure. Symptoms of a failing hip implant may include:

  • Pain
  • Swelling
  • Redness
  • Stiffness
  • Instability

In addition to these symptoms, the failure of the acetabular liner can lead to osteolysis, a condition that causes irreversible bone loss. Patients who fail to follow up with their surgeon may unknowingly suffer from this condition, which can worsen over time without detection. Regular monitoring is essential to avoid long-term damage.

Choose Rheingold Giuffra Ruffo Plotkin & Hellman LLP

If you have experienced complications from an Exactech Connexion GXL Acetabular Liner or any other defective hip implant, you may be eligible to file a claim. Victims of defective medical devices are entitled to compensation for their damages, including medical expenses, lost wages, and pain and suffering.

At Rheingold Giuffra Ruffo Plotkin & Hellman LLP, we are committed to advocating for patients who have been harmed by defective medical products. Our attorneys have a deep understanding of complex medical device litigation and offer personalized attention to each case.

To learn more about your legal options or to schedule a consultation, contact us at (212) 684-1880 or fill out our online contact form. We are here to help you seek justice.