Stryker® Hip Implants Attorneys Jacksonville

FDA Recall, Warning or Action: The FDA sent Stryker® (a major manufacturer of hip implants) an extremely stern, six-page letter detailing the problems that had been discovered with the company’s manufacturing process and other issues that need to be corrected immediately.

Whenever a manufacturer’s stake in the bottom line is diluted by their desire for maximizing profits, the public’s well-being is unjustly put at risk. Our law firm’s accident attorneys work closely with design engineers to identify dangerous drugs, inadequate warning labeling, incomplete healthcare guidance, and product design flaws as well as the subsequent adverse outcomes. In some cases the danger comes from the manufacturer’s failure to recognize dangerous situations or warn doctors of failed outcomes.

Side Effects of Stryker® Hip Implants Use

Stryker® is the worldwide market leader in total hip replacement products. The company achieved their position through innovation and by meeting requirements for hip arthroplasty products to help restore patients to normal daily activities. According to the FDA’s report, possible side effects and negative patient outcomes included:

  • Extreme Pain and Swelling
  • Difficulty Walking
  • Fractured Joint Implants
  • Squeaky or Clicking Joints
  • Improper Fitting of Implants

NOTE: Many lawsuits have already been filed by patients injured by the Stryker® hip implant systems and more are expected to come as patient injuries are revealed.

We often collaborate directly with other accomplished personal injury law firms to assure we attain an adequate restitution for victims of failed medical devices. If you or a loved one has been injured by or permanently damaged due the failure of a manufacturer or seller to exercise reasonable care (or to provide a safe product or service), contact us at 904-251-1111 or 1-800-251-1111 for a FREE initial consultation.

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