Attorney at Graves McLain Injury Lawyers
Practice Areas: Wrongful Death, Medical Malpractice, Bad Faith Insurance, Car Accidents, T-Bone Tractor-Trailer Accidents, Dangerous Drugs
If you’ve received a Stryker hip implant and later experienced pain, mobility issues, or even needed revision surgery, you’re not alone. Across Oklahoma and the U.S., patients have reported severe health problems linked to specific Stryker hip replacement systems.
Some of these implants have been recalled due to design flaws and material failures. If your hip implant caused complications, You may have grounds to sue and seek compensation.
This guide explains what Oklahoma residents need to know about Stryker hip implant issues, who qualifies to file a claim, and how product liability laws can help.
Stryker is a well-known manufacturer of orthopedic implants. Some of its most popular hip replacement systems, including the Rejuvenate, ABG II, and LFIT V40, were designed with modular components to improve flexibility during surgery.
Unfortunately, these same designs have led to serious problems for patients. Devices made from metal alloys can corrode or wear down over time, allowing harmful particles to enter the body.
The FDA recalled the Stryker Rejuvenate and ABG II modular-neck stems in 2012 due to corrosion and fretting, which may lead to serious tissue damage and metal toxicity.
These failures can cause inflammation and tissue damage, eventually leading to the implant loosening or breaking apart within the body.
Patients with faulty Stryker hip implants have reported a wide range of symptoms. Some of the most common include chronic pain in the hip or groin, reduced mobility, or unexpected swelling.
Other issues include:
These health problems can be painful, disruptive, and costly to treat.
Stryker Implant Model | Year Recalled | FDA Recall Reason | Reported Complications |
Rejuvenate Modular Neck | 2012 | Fretting and corrosion | Metallosis, pain, revision surgery |
ABG II Modular Stem | 2012 | Corrosion and early failure | Tissue damage, implant loosening |
LFIT V40 Femoral Head | 2016 | Taper lock failure | Dislocation, leg length discrepancy |
According to the National Joint Registry, metal-on-metal hip implants show higher failure rates compared to ceramic or polyethylene models.
In Oklahoma, patients harmed by a defective medical device can file a product liability claim. These claims typically fall under one or more of the following legal theories:
“Oklahoma’s product liability laws hold manufacturers strictly liable for defective medical devices that cause harm—even without proof of negligence.”
Oklahoma also follows a comparative negligence rule. This means your compensation may be reduced if you are found partly at fault for your injuries—for example, by delaying treatment.
You may qualify to file a lawsuit in Oklahoma if:
Even if your implant was not officially recalled, you could still be eligible to file a claim if it caused harm.
Filing a claim for a defective hip implant doesn’t happen overnight. It starts with a consultation, during which your attorney will review your medical history and implant information.
From there, the steps may include:
You generally have two years from the time you discovered the injury to file a claim in Oklahoma.
Depending on your circumstances, you may be able to recover compensation for:
You typically have 2 years from the date you discovered the injury or implant failure, per Oklahoma’s product liability laws. However, the timeline may vary depending on specific circumstances.
No. Even if your Stryker implant wasn’t part of an official recall, you may still be eligible if you experienced serious complications or needed revision surgery.
Metallosis occurs when metal particles from the implant enter surrounding tissues or the bloodstream, leading to inflammation, pain, or toxic reactions. It’s a known issue with metal-on-metal hip implants like some Stryker models.
Not always. Many claims are settled out of court. If your case proceeds to trial, your attorney will guide you through the process.
Hip implant lawsuits fall under product liability law, not medical malpractice. They focus on the manufacturer’s responsibility for a defective device, not a doctor’s actions.
Many Stryker lawsuits are part of national multidistrict litigation (MDL), but you may file an individual case depending on your circumstances and attorney’s guidance.
Stryker hip replacements have helped many people regain mobility—but for some, they’ve caused pain, complications, and the need for revision surgery. If you’ve been affected by a faulty implant in Oklahoma, you may have a legal right to seek compensation.
Every case is different. Speaking with a legal team that understands product liability law and Oklahoma’s legal system can help you make informed decisions about your next steps.
Graves McLain Injury Lawyers helps patients hold manufacturers accountable for dangerous medical devices. You don’t have to go through this alone. We’re here to support your recovery—legally and personally.
Please make an appointment for a free consultation with GRAVES MACLAIN INJURY LAWYERS right now to find out how they can support your future.
When injury victims need a law firm with a reputation for excellence, turn to Graves McLain Injury Lawyers. We are a top-rated personal injury firm determined to be the best. With decades of award-winning representation, our clients recover the compensation they need to put their lives back together.