Hip replacements are important surgeries and the patients count on the medical devices used to be safe. Individuals receiving hip implants should never have to worry that their medical device will break down and cause serious injuries.
That’s exactly what has happened with the Stryker Orthopaedic hip implants, Rejuvenate and ABG II. Even the Accolade V40 has begun to receive complaints.
If you have had a hip replacement surgery that used any of the mentioned Stryker Orthopaedic implants, then you could be eligible for financial compensation for your damages. Contact an experienced faulty medical device attorney today to discuss your legal options.
What are the Side Effects of a Bad Hip Replacement Surgery?
Faulty hip implants can cause a number of adverse side effects. Patients should never ignore pain that follows in the time after a surgery as it can be an indicator of a serious problem. Speak with your physician immediately if you notice any adverse effects from your hip implant surgery.
Here are some of the reported symptoms patients with faulty Stryker hip implants have experienced:
- Impacted mobility
- Sounds from the hip joint such as clicking, popping, grinding, or squeaking noises
- Pain in the hip, leg, or groin areas
- Hip joint swelling
- Metal poisoning
What are the Signs of Stryker Rejuvenate Hip Implant Metal Poisoning?
Of the adverse effects of the Stryker hip replacement perhaps the most serious is metal poisoning. The metal poisoning caused by hip implants is serious enough to severely injure and even kill some individuals. Symptoms that can indicate metal poisoning include vision or hearing changes, rashes on the skin, thyroid issues, poor kidney function, and cardiomyopathy.
Why Was the Stryker Hip Implant Recalled?
Stryker ABG II and Stryker Rejuvenate replacements were made with design flaws. Most hip implants have a one-piece neck and stem to fit the patient’s body. The Stryker hip implants were made for stability and designed to alleviate bone stress.
They were intended to be resistant to corrosion, but the junction of the metal pieces have been known to release iron and metal debris. These hip implants were approved and released by the 510(k) Premarket Notification Process. This means that they were never used on real people before being approved for the public.
Stryker used a company named Broadspire to help with the claims of faulty hip implants. Broadspire handled the cases of over one hundred thousand individuals that were given Stryker implants. As a third-party company, anything that the person shared with Broadspire can be used in subsequent litigation.
If you have concerns about the information given to Broadspire or any questions regarding your case, then you should speak with an Atlanta defective medical product attorney as soon as possible. The best Atlanta attorneys can help you determine if you have a valid claim.
Contact a Stryker Rejuvenate Hip Recall Lawyer in Atlanta
If you or a loved one have experienced harm from a Stryker hip implant, then you need legal help. A seasoned defective medical device attorney can help you pursue damages and financial compensation for your case.
Contact the legal team at Angell Law Firm today and let us get started fighting for your rights in court. We have locations in Atlanta and Toccoa, Georgia, as well as Greenville, South Carolina, to help you where you need us.
