Stryker Hip Replacement Lawsuit – Recall Injury Attorney

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Stryker Hip Recall Lawsuit | Stryker Injury Lawyer | Stryker FDA Recall Information

Do you or a loved one have a Stryker hip implant? Are you in pain or discomfort because of the hip implant? You may be entitled to compensation. Contact a personal injury lawyer today regarding your possible Stryker hip implant lawsuit.

Before its recall in July 2012, over 20,000 Stryker Rejuvanate modular-neck hip stems were sold in the United States by Stryker Orthopaedics. Thousands of patients who underwent hip replacement surgeries received these defective devices that consisted of metal components, thus increasing the risk of corrosion and metal toxicity. Because these systems were metal-on-metal implant devices, the parts had the potential to rub against one another, creating a friction that would often leave scraps and shards of metal to accumulate in the bloodstream and nearby tissues.

These Stryker hip implants have caused many patients to suffer from symptoms pertaining to metal ion poisoning, or metallosis and hip replacement failure, among other complications. In many instances, these patients have had to undergo one or more revision surgeries to correct the damage and remove the defective implants.

If you or someone you know are suffering from these side effects, you may be entitled to file a lawsuit against Stryker to obtain compensation for your injuries.

Complications Lead to Stryker Hip Implant Lawsuits

The Stryker hip replacement device was not the only system to cause serious injuries to patients. Similarly, the Biomet Magnum M2a devices, the DePuy Pinnacle and DePuy ASR hip replacements and the Wright Profemur and Wright Conserve hip replacement devices were all reportedly causing serious adverse side effects in patients undergoing seemingly routine implant procedures.

Since its recall in July 2012, the number of adverse events reported to the U.S. Food and Drug Administration (FDA) and used in lawsuits filed against Stryker has grown dramatically. Since the beginning of 2012, the FDA had received over 60 reports of tissue inflammation, metal corrosion and other serious complications from patients who received the Stryker hip implant. The overwhelming number of complaints led to increased attention regarding the devices and ultimately led to its recall.

According to a report from NorthJersey.com issued on February 28, 2013, over 80 lawsuits were currently pending in New Jersey Superior Court. Judge Brian R. Martinotti is to oversee the litigation.

In February 2013, a plaintiff filed a motion in federal court to coordinate similar pending claims in the U.S. District Court in the District of Minnesota. The creation of a multidistrict litigation would be beneficial for all plaintiffs as 10 out of 30 similar claims are pending at this location. It would also make the process smoother, as similar discoveries in different trials could be excluded.

Stryker Creates Claims Program

Stryker Orthopaedics has since taken action stemming from the thousands of claims brought forth by patients suffering from serious adverse health complications. [...]

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