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Stryker® Corporation is facing scrutiny regarding a component used in 14 of its hip replacement products, and hundreds of thousands of patients may be affected. The defective hip implant part—the LFIT™Anatomic CoCR V40™femoral head—is linked to a variety of serious medical complications, such as metal poisoning, severe pain, and implant failure requiring surgery to correct.
Our attorneys have experience helping patients harmed by defective medical devices, and we’re ready to provide a free, no-obligation consultation if you or a loved one:
The Stryker LFIT hip component is widely used. If you or a loved one have been affected, we’re here to help protect your rights. Our legal team can investigate your medical records or talk to your surgeon to help determine if you may be entitled to compensation. Call or contact us online now to get started—it only takes a few minutes to get the experienced help you deserve.
The Stryker hip issue is focused on a single component used in more than a dozen hip replacement products—the LFIT Anatomic CoCR (Cobalt Chromium) V40 femoral head. The part replicates the “ball” (or femoral head) at the top of the femur bone that forms a ball and socket hip joint and has failed at a higher-than-expected rate.
Patients with recalled Stryker hip replacement components may experience:
In some cases, surgery is required to correct Stryker hip replacement complications caused by the recalled LFIT Anatomic CoCR V40 femoral head.
Our law firm has the knowledge and resources to research defective hip implant cases, and we can determine your rights to compensation at no cost to you. If you or someone you love experienced serious hip replacement complications or were notified of a recall, contact our legal team to get help now.
Stryker® is a registered trademark of Stryker Corporation. LFIT™and V40™are trademarks of Stryker Corporation. This law firm is not associated with, sponsored by, or affiliated with Stryker Corporation.
Cases may be referred to another attorney or law firm.