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.


Medical Device Recall Issued for Baxter MiniCap Products

In February 2023, Baxter Healthcare Corporation issued an Urgent Medical Device Recall for the MiniCap product. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. This could lead to...

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Faulty Hip Replacement Devices

Joint replacement surgeries are becoming more common as medical technologies advance and people are living more active lives. A common joint to fail is the hip joint as it is the largest joint in the body.  According to the Agency for Healthcare Research and Quality,...

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Knee Replacement Medical Devices Recalls

Knee replacement, also called knee arthroplasty or total knee replacement, is a surgical procedure to resurface a knee damaged by various causes. Knee replacements are common as the knee is the largest joint in the body and having healthy knees is required to perform...

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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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