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New York Stryker Hip Implant Attorneys

Stryker Hip Implant Lawsuits

Medical device companies, such as Stryker, quietly groom doctors to promote their products. These are known as “key opinion leaders.” Stryker had “hot spots” in Florida and Oklahoma, but we now know doctors in Northern New Jersey and Southern New York liked the Stryker line. Many doctors switched to Stryker Rejuvenate and ABG II after the DePuy ASR recall. Stryker falsely touted these as not being metal-on-metal.

Helping Clients Across the Nation

Our New York defective hip implant attorneys aggressively litigate medical device cases based on our firm’s extensive experience in other faulty medical device cases. Call (212) 684-1880 to learn more.

The Rejuvenate & ABG II Implant

The Stryker Rejuvenate and ABG II systems were recalled in 2012 for metallosis and failure. Stryker’s patented titanium TMFZ femoral stem and cobalt/chrome neck create a corrosive reaction which poisons the patient’s bones and tissues. Even before the recall, Stryker acknowledged this general problem of mismatched metals in sales material.

Stryker co-marketed the implant with Howmedica, a New Jersey company. This means we can file any client’s case in New Jersey. Medical device litigation in New Jersey courts can provide strategic options not available in other state or federal courts.

The LFIT V40 CoCR Hip Implant

Canada has recalled (and Australia has warned about) the LFIT CoCr V40 Stryker femoral heads. In some implants there is excessive wear on the trunnion and the implant fails. Patients experience intense pain and instability requiring revision surgery. Orthopedics may currently be thinking that this is “typical” wear and tell but it is not. The implant should last at least ten years, but is lasting for half that time. These heads are used interchangeably in any of Stryker’s hip implants from before 2011.

Symptoms Associated with a Failing stryker Implant:

  • Increase of pain in the hip joint
  • Soreness after extended exertion
  • X-rays or MRI scans showing fluid collection or “pseudotumors”
  • Blood tests showing elevated levels of cobalt or chromium

Contact Us for a Case Evaluation

Our New York defective hip replacement lawyers work closely with clients, their families and their physicians. Physicians rarely understand the liability aspects of your claim, and we take the time to explain to them how a company’s defective product was able to be marketed while hiding its shortcomings.

We can discuss with you issues such as:

  • How to identify if you have a recalled product
  • What are the serum tests being done for metal particle disease, also known as metallosis, cobalt poisoning and chromium poisoning
  • Preservation of hip implant hardware as evidence
  • What are the litigation and settlement prospects, and how these directly relate to your specific injury

Our experienced lawyers help victims of defective medical devices nationwide. To discuss your case with our team, call (212) 684-1880 or contact us online