Leading Justice is a full-service marketing company working with law firms on a cash-buy basis to sign up fully-qualified, fraud-free Stryker hip implant cases. Here at Leading Justice, we can custom-tailor your firm’s Stryker LFIT hip replacement advertising needs and help you sign up cases via internal cash buys. Our clients simply pay an agency fee to cover the cost of Stryker advertising, plus a fee for each case we sign, and any data we generate for your firm belongs to you. We also cross-qualify all of our contacts, which means any data we generate that isn’t eligible for the target campaign is reviewed to determine whether it qualifies for another type of claim. By using advanced approaches to target contacts specifically related to Stryker hip implants and side effects like chronic pain, metal blood poisoning, and the need for revision surgery, Leading Justice will increase your firm’s Stryker LFIT Femoral Head implant caseload. If you are interested in helping victims of alleged Stryker hip replacement side effects, our extensive consumer reach and direct advertising strategies at Leading Justice give you the competitive edge and confidence to allocate your full budget, and rest easy knowing that your money is being used in the best way possible.
Each and every law firm we work with at Leading Justice plays an important role in determining how we classify claims as qualified or not. While our experience working with plaintiff law firms help us recognize a great case when we see one, we will customize our Stryker hip implant case intake specifications to the exact criteria you are seeking. So, if your firm has specific Stryker LFIT Femoral Head qualifying case criteria you would like us to use, we can train our intake specialists to apply the criteria to each phone call and email they receive. By getting rid of the middle man, Leading Justice offers clients an opportunity for internal cash buys of Stryker hip implant data with no chance of fraud.
Stryker LFIT COCR Femoral Head Side Effect Litigation
The LFIT Anatomic COCR V40 Femoral Head, a metal-on-metal hip implant manufactured by medical device maker Stryker Orthopaedics, has been linked to reports of catastrophic device failure and devastating injury in patients who have received the artificial hip. According to reports, the cobalt and chromium heads of the LFIT V40 implant may be prone to corrosion, to the point where the femoral head actually separates from the stem, a side effect known as “spontaneous dissociation.” Patients with Stryker LFIT hip implants who suffer spontaneous dissociation require immediate surgery to remove both the head and stem components of the hip replacement system. In other cases, corrosion of the Stryker hip may release toxic amounts of cobalt and chromium into the patient’s body, resulting in metallosis, or metal blood poisoning, which can cause systemic injury in affected individuals.
In 2016, Stryker issued a voluntary recall of its LFIT Femoral Heads after patients reported suffering debilitating pain and toxic levels of cobalt and chromium in their bodies, side effects that have been associated with the artificial hip implant. In many cases, alleged defects in the design of the artificial hip replacement system have made it necessary for patients to undergo a second hip revision surgery to remove the Stryker implant. This unexpectedly high rate of failure of the Stryker hips has led recipients of the artificial hip implant to pursue legal claims against Stryker Orthopaedics, alleging such injuries as debilitating pain, reduced mobility, cobalt poisoning, broken bones, tissue death, dislocation of the femoral head from the hip stem, and the need for multiple surgeries to remove the defective implants. According to these claims, Stryker was negligent in failing to properly test its LFIT COCR V40 Femoral Head devices, and in failing to warn doctors and patients about the risks associated with the implants.