Problems with Zimmer Durom Cup hip replacement have resulted in revision surgeries. Discuss any device failure with our attorneys.

The Food and Drug Administration has received a number of reports from surgeons who have indicated that they were required to perform revision surgeries on patients with the Zimmer Durom Cup Hip.

In that correspondence, some have indicated that during the Zimmer hip replacement revision surgery with the Durom cup, health care professionals noticed that the acetabular component of the Zimmer Durom Cup had loosened or become displaced.

This situation with the Zimmer Durom hip replacement may ultimately result in Zimmer hip replacement patients having to have a hip revision surgery.

Hip pain after the replacement surgery may indicate a faulty hip implant, broken hip implant, or defective hip implant.

If you have experienced this situation with the Zimmer Durom hip replacement, contact your orthopedic surgeons or the hospital where their hip replacement surgery took place to determine if the Zimmer Durom Cup Hip Implant was used in your hip replacement surgery.

Read the FDA recall information.

Our defective drug and medical device lawyers have been investigating the durom implant and will be seeking Zimmer settlements for patients implanted with the defective Zimmer Durom Cup Hip Implants.

If your Zimmer Durom hip replacement failed to work, caused discomfort, or required replacement, please complete the form below to receive a free review of your case from our lawyers. A representative of our firm will be in touch shortly.

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Device Failures

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Loose Cup

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Lawsuit Resources

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