All eight lawsuits currently pending against the company were filed in New Jersey Superior Court, Bergen County and similarly allege that the company negligently developed, tested, manufactured, distributed, and sold its defective Rejuvenate System.
New York, NY (PRWEB) September 13, 2012
Additional Stryker hip recall lawsuits have been filed against Stryker Orthopaedics, manufacturer of the recalled Rejuvenate and ABG II modular-neck hip stems, Bernstein Liebhard LLP reports. The South Florida Sun Sentinel reported on seven recently filed lawsuits against the medical device manufacturer over the recalled devices.* According to the news report, the seven new lawsuits currently pending against the company were filed in New Jersey Superior Court and similarly allege that the company negligently tested, manufactured, distributed and sold its defective Rejuvenate System. The seven new plaintiffs had to undergo revision surgery to remove the devices. The South Florida Sun Sentinel also noted that a large number of patients who received the Rejuvenate have suffered metal toxicity.
“We believe this is just the beginning of litigation against Stryker. Many recipients of the recalled Stryker implants have experienced symptoms of hip implant failure yet still don’t even know that their failing implant was recalled. As more patients are notified of the recall, we are hopeful they will take steps to protect their legal rights. We continue to receive calls from Stryker hip implant recipients on an almost daily basis,” said Bernstein Liebhard LLP, a nationwide law firm representing individuals in lawsuits against a variety of metal hip implant manufacturers. The Firm is currently offering free and confidential case reviews to individuals who received either a Stryker Rejuvenate or ABG II modular-neck stem hip implant and experienced side effects.
Stryker Hip Recall Lawsuits Likely To Rise
In July 2012, Stryker Orthopaedics recalled its Rejuvenate and ABG II modular-neck hip stems – components used in many of the company’s hip implant systems. Approximately 20,000 of the recalled devices were sold in the United States. According to the company, the recall was initiated due to elevated risks of “fretting and/or corrosion at or about the modular-neck junction, which may result in adverse local tissue reactions manifesting with pain and/or swelling.”**
In addition to providing a wealth of information related to the recall on the Firm’s website, the lawyers at Bernstein Liebhard LLP are currently evaluating potential Stryker hip recall lawsuit claims. Those who received the recalled Stryker Rejuvenate and ABG II modular-neck hip stems and have suffered damages as a result of being implanted with the devices may be entitled to compensation for medical expenses, pain and suffering, lost wages and other injuries. Learn more by watching this Stryker hip recall lawsuit video, or by visiting our website, http://www.consumerinjurylawyers.com/Stryker-Hip-Recall-Lawsuit. For more information, contact a lawyer at Bernstein Liebhard LLP today at (877) 779-1414.
About Bernstein Liebhard LLP
Bernstein Liebhard LLP is a New York-based law firm exclusively representing injured persons in complex individual and class action lawsuits nationwide since 1993, including those who have been harmed by dangerous drugs, defective medical devices and consumer products. The firm has been named by The National Law Journal to the “Plaintiffs’ Hot List,” recognizing the top plaintiffs’ firms in the country, for the past nine consecutive years. Only two firms in the country have been selected for the Hot List nine years in a row.
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ATTORNEY ADVERTISING. © 2012 Bernstein Liebhard LLP. The law firm responsible for this advertisement is Bernstein Liebhard LLP, 10 East 40th Street, New York, New York 10016, (212) 779-1414. The lawyer responsible for this advertisement in the State of Connecticut is Amy L. Abate. Prior results do not guarantee or predict a similar outcome with respect to any future matter.
Felecia L. Stern, Esq.
Bernstein Liebhard LLP