Attorney at Graves McLain Injury Lawyers
Practice Areas: Wrongful Death, Medical Malpractice, Bad Faith Insurance, Car Accidents, T-Bone Tractor-Trailer Accidents, Dangerous Drugs
Hip replacements are designed to relieve pain and restore mobility, but not every implant delivers on this promise. Across Oklahoma, some patients who received Stryker hip replacements have reported painful complications, unexpected failures, and the need for follow-up surgeries. These problems often appear months or even years after the original procedure, catching patients off guard and disrupting their recovery.
If you or a loved one has experienced issues after receiving a Stryker hip implant, you’re not alone. Specific models have been linked to serious design flaws, and legal action is underway across the country.
In this post, we’ll explain what’s gone wrong, how these implants are affecting Oklahoma patients, and what legal steps may be available to hold the manufacturer accountable.
Stryker Corporation has manufactured several hip replacement devices that have triggered safety alerts and lawsuits. Early models, such as the Rejuvenate and ABG II, were recalled due to reports of metal corrosion and premature failure. More recently, the LFIT Anatomic V40 The femoral head has been flagged for similar issues.
In 2016, Australian health officials issued a hazard alert about the LFIT V40 component, citing a risk of dislocation, bone fractures, and early failure.
These components are used in many total hip replacements and are supposed to last for years. Unfortunately, problems with the way they fit together have led to unexpected breakdowns and complications.
Many patients begin to notice symptoms months or even years after surgery. These signs often include persistent pain, swelling, clicking in the joint, or difficulty walking.
In more severe cases, the implant may fail, leading to:
Stryker has paid over $1 billion in settlements for claims involving its Rejuvenate and ABG II models, which had similar design flaws.
“The physical and emotional toll of dealing with hip implant complications can be overwhelming—especially when the device was expected to provide lasting relief
Model | Problem Areas | Resulting Complications |
| Rejuvenate | Corrosion at modular neck | Metal poisoning, tissue damage |
| ABG II | Early loosening, inflammation | Loss of mobility, revision surgery |
| LFIT V40 Femoral Head | Taper lock issues, disassociation | Dislocation, bone damage |
If a faulty hip implant harmed you, you may be eligible to file a product liability claim under Oklahoma law. These cases are often based on design defects, manufacturing flaws, or a company’s failure to warn about known risks.
To move forward with a claim, you’ll typically need to show:
In Oklahoma, you generally have two years from the time you become aware of the injury to file a product liability claim.
This time limit is strict, so it’s essential to act promptly, even if your surgery happened years ago.
Product liability cases involving medical devices can be complex and challenging. Medical records must be reviewed, expert opinions may be needed, and large corporations like Stryker will likely fight the claim.
That’s where an experienced Oklahoma product liability lawyer can make a difference. A qualified attorney can:
Choosing a firm based in Oklahoma means your legal team is familiar with local laws, court systems, and filing deadlines. At Graves McLain Injury Lawyers, we’ve worked with clients across the state who defective medical devices have harmed.
Reports submitted to the FDA have flagged multiple safety concerns with Stryker hip implants, including taper lock failures and metal-related reactions.
Our firm is well-versed in these issues and knows how to construct a strong case, supported by clear documentation and expert testimony.
TheStryker’s Rejuvenate, ABG II, and LFIT V40 femoral heads have all been linked to safety issues, including early failure and metal-related complications, leading to recalls and ongoing product liability lawsuits.
Request your surgical records from your hospital or orthopedic surgeon. These documents will list the manufacturer and model of the implant used during your hip replacement procedure.
Common signs include ongoing hip pain, swelling, joint instability, clicking sounds, leg length differences, or the need for a second (revision) surgery after the initial implant procedure.
Yes. Under Oklahoma law, you typically have two years from when you became aware of the injury to file a product liability lawsuit. It’s essential to act quickly.
Possibly. If your symptoms or diagnosis have only recently revealed the problem, you may still be within the legal time frame. Consult an attorney to understand your specific situation.
Yes. A local attorney is familiar with Oklahoma’s legal process, court deadlines, and the application of state laws to product liability claims involving defective hip implants.
Stryker hip implants have been linked to serious health problems for patients across the country, including many right here in Oklahoma If you’ve suffered complications, you have the right to explore your legal options.
The first step is to understand your device and document your symptoms. The next step is speaking with a legal team that knows how to hold manufacturers accountable.
At Graves McLain Injury Lawyers, we’re committed to helping Oklahomans recover from medical device injuries. If you’re facing pain, mobility issues, or revision surgery, we can review your case and explain your options with no upfront cost.
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.
