In 2008, Zimmer, Inc. issued a voluntary recall of the Zimmer® Durom Acetabular Component (Durom Cup). This component was designed to help individuals with non-inflammatory degenerative joint disease. However, many patients implanted with the Zimmer® Durom Cup were later forced to have this component surgically removed as a result of severe pain and other serious health complications.
While a voluntary or mandated recall of the Zimmer® M/L Taper Prosthesis with Kinectiv® Technology has not yet been issued, Ward Black Law is already beginning to review cases of patients who have suffered hip implant failure or other significant health consequences after being implanted with this device.
If you or a family member has suffered severe injury due to the malfunction of a Zimmer® Durom Cup or the Zimmer® M/L Taper Prosthesis with Kinectiv® Technology, please contact Ward Black Law for a free consultation, by phone: 336-333-2244 or toll-free: 1-800-531-9191. You may also reach Ward Black Law by email: firstname.lastname@example.org or by online inquiry.
Have you or a loved one recently undergone revision surgery as a result of complications with a Zimmer® hip implant? If so, an informed attorney may be able to help you determine the viability of a potential hip implant failure claim. The attorneys at Ward Black Law in Greensboro, North Carolina, have the knowledge and experience you can trust to handle these types of claims.
For more information on what the Federal Drug Administration has to say about metal-on-metal hip devices, such as the Zimmer® Durom Cup or the Zimmer® M/L Taper Prosthesis with Kinectiv® Modular Neck Technology, click here.
If you have questions about your rights regarding a hip implant failure claim, please contact Ward Black Law for a free consultation: 336-333-2244 or toll-free: 1-800-531-9191. You may also reach Ward Black Law by email: email@example.com or by online inquiry.