In 2012, the Stryker Osteonics Corporation recalled the ABG II and the Rejuvenate hip implants-two of its most popular artificial joint impact devices-over serious concerns regarding patient safety. A few years later, Stryker voluntarily recalled its LFIT Anatomic V40 femoral head devices over similar concerns.
Thousands of patients have suffered severe side effects following hip implant surgeries, including fractured femurs and pelvic bones, joint instability, hip dislocation, cognitive problems, severe pain, and other medical conditions.
If you a person has undergone a hip replacement procedure and, afterward, suffered any of these symptoms, or if a person has been forced to undergo a hip replacement or revision surgery after receiving a Stryker hip implant, the person may be entitled to compensation for one's injuries. To see whether the person has a claim, one should contact the experienced personal injury lawyers at Arnold & Smith, PLLC to schedule a free consultation. Our lawyers have assisted many families in making informed decisions about pursuing justice and obtaining the compensation they deserve for their injuries.
Stryker Artificial Hip Implant Systems Pose Danger to RecipientsOver a decade ago, the Stryker Corporation developed a range of metal-on-metal hip replacement devices. The company promised surgeons that its devices promised patients more options and the ability to customize their treatment. The company developed artificial hip joints with an acetabulum socket-a pelvic concave indentation with a femoral head (ball)-available in assorted sizes.
Unfortunately, patients who received the implants complained that the hip devices caused serious injuries. Some patients reported complications immediately after receiving metal-on-metal hip implants. Other patients began reporting injuries and symptoms months after receiving the implants.
Defective Stryker Artificial Hip Implants Cause a Range of InjuriesIn numerous legal actions against Stryker, claimants have alleged that components from defective metal-on-metal hip implants break down after implantation. The metal rubs on metal, creating flakes of metal that break off into a patient's body. This flaking and corrosion can cause several dangerous medical conditions.
After learning about the conditions, the Stryker company sent out an urgent safety notice alerting professionals in the medical community that components of the devices had a high failure rate that produce serious side effects, including:
A person who has been forced to undergo a Stryker hip implant revision surgery may be entitled to pursue a claim for damages. In many cases, persons who have already received a revision surgery have suffered injuries that created a right to pursue compensation. In order to prove a claim, an affected person must demonstrate, with testimony and evidence, that one's damages and injuries were proximately caused by the defective hip implant.
Under North Carolina law, manufacturers of defective products are liable for any injuries caused by the defective products. These actions are called "products liability" claims. North Carolina's "Products Liability" statute contains specific requirements for pursuing such claims. The professionals at Arnold & Smith, PLLC can assist persons in pursuing products liability claims.
Contact Our Experienced Charlotte Product Liability FirmIf you or someone you love has undergone a hip implant revision procedure necessitated by a faulty Stryker hip implant, it is essential that the affected person speak with a lawyer as soon as possible. Contact our Charlotte personal injury law firm to schedule a free initial consultation today.