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Stryker Hip Warning

The Stryker Rejuvenate and ABG II are popular metal-on-metal hip replacement systems that have been used in more than 20,000 patients since released in 2010. However, the company recently issued a Stryker hip warning and recall due to serious health concerns.

If you or someone you love received a Stryker hip implant, it is important to speak with your doctor and an attorney about your options as soon as possible.

In April of 2012, a Stryker hip warning letter sent to physicians cautioned that the Rejuvenate and ABG II hip implants could experience corrosion and fretting, releasing metallic shavings into the bloodstream and surrounding tissue.

Then, on July 6, 2012, Stryker recalled the Rejuvenate and ABG II modular-neck hip implant systems. Although the company has offered reimbursement for testing and removal, they have not offered patients full compensation for metallic poisoning or their resulting damages.

Since Stryker did not properly test these devices or warn patients of the dangers of metallic poisoning, they are liable for the damages caused. Attorneys are currently helping those affected file claims.

If you or a loved one received a Rejuvenate or ABG II hip implant, it is important to know your legal and medical options under the Stryker Hip Warning. Contact us today to speak with a lawyer.

The Stryker Rejuvenate and ABG II hip implants use a modular system which was designed to provide a better, more comfortable patient fit by allowing surgeons to use different-sized, interchangeable necks and stems.

However, wear and movement between the joined metal components, made of chromium, cobalt and titanium, can cause fretting and corrosion.

Recent studies have shown that metal shavings released into tissue, bone or the bloodstream can have severe side effects such as allergic reactions, bone loss, soft tissue damage, vision or hearing problems or even tumors and cancer. 

No one should file a lawsuit unless a company’s negligence has caused them harm. An attorney can explain how Stryker was negligent in not properly testing these devices or warning patients of the dangers.

The signs of metallic poisoning can take years to surface. However, patients should monitor for symptoms such as pain, inflammation, swelling, tissue damage, vision problems or tumors. Those affected will likely have to undergo revision surgery to remove and replace the device.

Attorneys have helped thousands of families recover after drug and medical device injuries. These same attorneys are available to discuss the current Stryker Hip warning and help with your case today. They can let you know how much it may be worth and how long you have to take action.

Lawsuits such as this for defective medical devices can be very complicated. Make sure any attorney you choose is extremely qualified, has experience fighting large medical device companies, and has the resources to finish your case.

The Hip Defect Resource Center works only with lawyers who have already handled Stryker hip lawsuits to make sure your case is handled properly and you recover quickly.

Contact us today for more information on the side effects, research and litigation related to Stryker hip implants, or to speak with a lawyer. We are available 24 hours a day to provide help.

 

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