During these unprecedented times, Clark, Perdue, & List Co, LPA is here to fully support your needs in a timely and safe manner. COVID-19 should not affect your ability to investigate a personal injury case. We currently remain open and are still accepting new cases. With your safety top of mind, we are scheduling all meetings via telephone or video conference at this time.

Defective Hip Replacements: Stryker and Biomet Suits Continue

Clark, Perdue & List continues to investigate claims for defective hip replacements involving Stryker Rejuvenate and Biomet Magnum hip implants. It is estimated that some 20,000 Stryker hip implants have been recalled and the implant devices are failing every day. Thousands of new Stryker claimants are expected to require legal representation for their injury claims.

On November 20, 2013, it was announced that DePuy ASR hip implant cases in which revision surgery had occurred have settled for $2.475 billion. Thousands of non-revision DePuy ASR cases are still pending. According to industry reports, over 40% of all DePuy ASR hip implants have failed prematurely resulting in revision surgery. In addition, 5000 claims are pending against DePuy (Johnson & Johnson) regarding failed Pinnacle hips. The number of claims continues to grow.

Key experts believe that all metal on metal (MoM) hip implants present an inherent and unreasonably unsafe risk to hip implant patients. The experts believe the devices were not property tested and offer no real benefit to the patient when compared to other hip implants such as metal-on-poly hips.

In all three litigations, it has become apparent that the defendant corporations are unwilling to adequately compensate individuals injured by these defective hip replacements unless revision surgery has taken place.

Contact An Attorney

If you or a loved one has received a Stryker Rejuvenate or Biomet Magnum hip implant and that implant has failed, contact the Ohio defective hip implant attorneys at Clark, Perdue & List.


Knee & Ankle Joint Replacement Recall

The medical device company, Exactech, has expanded its recall of some of its knee and ankle medical implants due to improper vacuum sealed bags that did not meet specifications.  The products were packaged without an additional layer of ethylene vinyl alcohol that further augments oxygen resistance.

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Paragard IUD Lawsuit Update

For more than a year, Clark Perdue has been investigating and pursuing claims for women who have suffered injury as a result of the Paragard® IUD.  This is a brief update on the status of these case. In December 2020, the the United States Judicial Panel on...

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Never Events & Medical Malpractice Claims

Do you need advice from a medical malpractice attorney in Columbus? Medical treatment is never without risk, but the benefits should outweigh the risks. In most cases, it does – but mistakes happen. Some don’t lead to serious harm, but there are certain errors that no...

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ParaGard® Benefits and Dangers

ParaGard® is an intrauterine device (IUD) that can provide long-term birth control. It is sometimes referred to as a nonhormonal IUD option. Paragard® is indicated for prevention of pregnancy in females of reproductive potential for up to 10 years. What is ParaGard®?...

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NuVasive MAGEC Recall

NuVasive created the MAGEC (Magnetic Expansion Control) to offer a safer treatment option to children with scoliosis. Scoliosis can develop during childhood and is an abnormal curvature of the spine. Severe scoliosis requires children to undergo surgery to implant...

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Stryker LFIT V40 Femoral Head Recall

On May 22, 2018, Stryker Orthopedics updated its Stryker LFIT V40 Femoral Head Recall to include eight (8) additional catalog numbers.  The original recall occurred in August 2016 and included seven (7) catalog numbers which represented close to 45,000 devices in...

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