When hip replacement devices fail, the results can be catastrophic — causing chronic pain, tissue damage, metallosis, or the need for revision surgery. Several manufacturers have recalled defective or poorly designed hip and metal-on-metal implants, exposing thousands of patients to serious health risks.
At Salenger, Sack, Kimmel & Bavaro (SSKB), we are investigating claims on behalf of patients nationwide who suffered complications after receiving defective hip implants — including those made by Zimmer Biomet, Smith & Nephew, Stryker, Encore, and OMNILife Science.
Joint replacement surgery, or arthroplasty, involves removing damaged cartilage and replacing it with an artificial implant made of metal, ceramic, or plastic. The goal is to restore movement, reduce pain, and improve quality of life. Unfortunately, not all implants perform as intended.
On July 2, 2024, Zimmer Biomet issued a voluntary recall of its CPT Hip System Femoral Stem 12/14 Neck Taper after reports of mechanical failure at the modular junction. The manufacturer announced plans to phase out sales by the end of 2024.
Patients implanted with this device have reported:
This recall adds to Zimmer Biomet’s history of product-safety issues, including prior settlements involving the Durom Cup and M2a Magnum hip implants. Our firm is now actively reviewing cases involving CPT Hip System failures, particularly where revision surgery occurred less than 13 years after implantation.
Although there is no consolidated litigation for Encore Metal-on-Metal hips, SSKB and partner counsel have successfully resolved individual cases involving these defective devices.
Patients experienced:
If your Encore implant failed or caused elevated cobalt/chromium ion levels, our attorneys can help evaluate your claim.
While no consolidated federal litigation currently exists for these modular-neck hip replacements, we have successfully resolved numerous claims involving corrosion and mechanical failure at the modular neck junction.
Reported issues include:
Patients who underwent revision surgery within 12 years of their initial implant may still qualify for compensation.
The Smith & Nephew Emperion Femoral Stem has not been part of a formal MDL, but numerous patients experienced fractures of the femoral stem leading to urgent revision surgery. These fractures often occur without trauma, suggesting a design or material-strength defect. If you suffered a sudden fracture of your Emperion stem, contact our team to discuss a potential legal claim.
A now-closed Multidistrict Litigation (MDL) in Maryland addressed thousands of cases involving Smith & Nephew R3 Metal-on-Metal and Birmingham Total Hip Replacements.
Although the MDL is virtually closed, SSKB continues to accept cases where:
We have successfully resolved similar claims and continue to represent patients nationwide affected by toxic metal debris and early device failure.
The Stryker LFIT V40 MDL No. 2768 (U.S. District Court – Massachusetts) and related New Jersey state consolidation in Bergen County involved thousands of claims over catastrophic disassociation of the femoral head and corrosion at the taper junction.
Two major confidential settlements were reached in 2018 and 2021, with Ellen Relkin playing a key negotiating role.
While most litigation has concluded, SSKB is still accepting claims for patients who:
Even though many metal-on-metal failures occurred more than a decade ago, patients revised recently may still be eligible.
If you or a loved one has experienced complications from a hip or joint replacement, don’t wait to seek legal help.
Contact Salenger, Sack, Kimmel & Bavaro today for a FREE consultation.
Call (800) 675-8556 or contact us online to get started.
If you’ve received any recalled or metal-on-metal hip implant, be alert for signs of failure, including:
If you are unsure which implant you received, our attorneys can help review your surgical and implant records.
Many metal-on-metal implants release microscopic debris of cobalt and chromium, which can accumulate in soft tissue and bloodstream, causing metallosis — a serious, sometimes irreversible condition.
Symptoms include:
Failure to diagnose metallosis can result in permanent disability. If blood tests confirm elevated metal ions, it is important to seek legal and medical review immediately.
Victims of defective hip implants may be eligible for compensation for:
Our attorneys investigate claims based on product liability, defective design, failure to warn, negligence, and breach of warranty. In cases involving severe harm or wrongful death, families may also pursue survivorship or wrongful-death claims.
You may qualify if:
If your case meets these criteria, our team will provide a free evaluation to determine eligibility for legal action.
If you or a loved one required revision surgery after a hip replacement involving any recalled or metal-on-metal device, contact our legal team today.
📞 Call (800) 993-8888
📩 Submit our Secure Online Form for a Free, Confidential Case Evaluation
Our attorneys will review your implant details, medical history, and revision records to determine eligibility for compensation.
Is there a time limit to file a claim?
Yes. Statutes of limitations vary by state, often ranging from 2 to 3 years from the date of revision surgery or discovery of the defect. Contact us promptly to preserve your rights.
Do I need my implant card or model number?
Not necessarily. We can help obtain your implant information from hospital or surgeon records.
What if my implant failed more than 10 years ago?
Some claims may still qualify if revision occurred within 13 years or if delayed discovery can be proven. We can assess this during your free consultation.
Are there active settlements?
While most large MDLs have concluded, individual settlements remain available for qualifying Zimmer Biomet, Stryker, and Smith & Nephew cases.
If you experienced complications from a hip implant recall or defective knee replacement, you may have a valid claim. Our team of hip replacement lawyers, knee replacement attorneys, and medical device litigation experts are here to help.
📞 Call (800) 675-8556 or submit your free case review online.