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Stryker Hip Replacements

On November 3, 2014, Stryker announced a settlement of the lawsuits involving patients whose Rejuvenate or ABG II hip replacement systems were revised prior to November 3, 2014. This settlement was valued at over $1 billion. Stryker's liability is not capped. It is expected that the total amount of payments under the settlement will far exceed $1 billion dollars. Payments under the settlement program are projected for disbursement at the end of 2015.

Why Were These Stryker Hip Replacement Systems Recalled?

Physicians and health regulators have focused substantial attention on the dangers to patients from the release of tiny metallic particles from all-metal (also called metal-on-metal) hip implants.

Stryker's Rejuvenate and ABG II modular-neck hip stem systems contain components made of chromium, cobalt, and titanium. Friction created by the normal movement of the components that make up Stryker hip replacement systems can release microscopic shavings and metal debris into the surrounding tissue and blood. This can lead to a condition called metallosis, which is characterized by painful, inflammatory reactions in the tissue and a high blood-metal count.

What Are The Symptoms of Patients Injured by The Recalled Stryker Hips?

Patients who have received Stryker's Rejuvenate and ABG II hip systems should be aware of the symptoms which may indicate that their devices are not functioning properly. Common symptoms include:

Regular and prolonged pain in the groin, hip, or leg;
Swelling at or near the hip joint; or
Numbness
A limp or a change in walking ability.
Skin Rash
Thyroid Dysfunction
Metallosis/ Blood Poisoning
Neurological changes such as auditory or visual impairments

In April 2012, Stryker issued an "Urgent Safety Alert" to surgeons for the two hip replacement systems. The alert listed "excessive metal debris and/or ion generation" as one of the safety risks to patients. According to Stryker's Safety Alert, the following problems can result:

Metallosis (release of metal ions into the tissue and bloodstream);
Necrosis (premature tissue death);
Osteolysis (bone dissolution); and
Pain and loosening of the hip implant requiring revision surgery.

You should contact an attorney at your earliest convenience. You are invited to contact our law firm today by using the form below or by calling us directly at 1-800-229-7989.

If your Stryker Rejuvenate or ABG II hip system failed and you underwent revision surgery to replace it after November 3, 2014, or if it fails in the future, you are not eligible for payment under the settlement announced last year.

However, you retain your rights to file a lawsuit against Stryker and seek compensation for the injuries you suffered as result of the implant failing. Keep in mind though, the statute of limitations (the deadline to file a lawsuit) varies by state and may preclude you from filing a claim if you do not contact an attorney promptly.

If you or a family member have experienced problems with a Stryker Rejuvenate Modular Primary Hip System or a Stryker AGB II Modular Hip System replacement implant, or have been told your implant should be replaced, please call us at 1-800-229-7989.

We welcome the opportunity to review your claim. We will respond promptly and there is no charge or obligation on your part for our evaluation of your case.

Visit here to learn more about our National Hip Implant Representation.

For more information visit https://badhiplegalhelp.com/