Many patients implanted with a Zimmer® hip replacement, such as the Zimmer® M/L Taper Prosthesis with Kinectiv® Technology, suffer from debilitating hip pain as a result of the implanted hip device.
The Zimmer® M/L Taper Prosthesis with Kinectiv® Technology is a hip replacement system featuring a variety of modular metal components, designed to be more durable and adjustable than other hip devices. Today, however, the Zimmer® Kinectiv® hip implant is linked to a range of serious health issues, including:
Metallosis (metal poisoning)
Loosening and dislocation of the hip joint
Many Zimmer® Kinectiv® hip patients experience such severe hip problems that they are forced to undergo costly, complicated revision surgery to replace the original artificial hip.
Individuals implanted with a Zimmer® Kinectiv® hip device, and exhibiting symptoms such as severe pain, should seek prompt medical attention and expert legal counsel as soon as they are able.
Note: Reports of severe pain and other serious side effects have also been reported in patients implanted with the Zimmer® Durom Acetabular Component (also known as the Zimmer® Durom Cup). The wide range of health complications associated with this product led Zimmer, Inc. to issue a voluntary recall of the Durom Cup component. A recall has not yet been issued for the Zimmer® Kinectiv® hip device and related device components.
The experienced attorneys at Ward Black Law in Greensboro, N.C., have years of experience representing clients and victims of dangerous medical devices and products, such as the Zimmer® M/L Taper Prosthesis with Kinectiv® Technology. Our legal team is available to answer your questions and conduct a free case review. Call Ward Black Law today at 336-333-2244, or toll-free at 1-877-256-1214. You may also reach Ward Black Law by email or online inquiry.