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Stryker LFIT V40 Femoral Head Hip Implant

Clark, Perdue & List is investigating injury claims related to failure of the Stryker LFIT V40 Femoral Head Hip Implant

Stryker LFIT V40 Femoral Head Hip Implant is used in hip replacement surgeries. According the the Australian equivalent of the FDA in the United States, the Stryker LFIT has “a higher than expected incidence of taper lock failures.”

The Stryker hip implant system features three components. The femoral neck is inserted into the thigh bone. The femoral head is the ball which rotates inside the hip socket. The taper lock connects the femoral neck to the femoral head. Failure of the taper lock could cause severe complications, including the need for additional surgery.

Our unsafe medical device lawyers are investigating potential claims of patients who were implanted with the Stryker LFIT V40 Femoral Head hip implant and who have suffered complications. Contact us for a free consultation.

If you or a loved one has been harmed by a unsafe medical device, contact us for a free consultation.

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BLOG POSTS ABOUT DEFECTIVE HIP REPLACEMENTS

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 ...
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Stryker hip implant settlement announced

A national settlement of Stryker hip replacment claims was announced yesterday. The total estimated settlement for the defective hip implants may exceed $1 billion.The settlement provides for the largest base ...
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Stryker Defective Hip Replacements Bellwether Trials Set

The first bellwether trials in the Stryker defective hip replacements litigation have been scheduled. Two trials have been scheduled for June 15, 2015 and July 13, 2015 in the Superior ...
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Defective Hip Replacements: Biomet Agrees to Settlements

Indiana-based Biomet, Inc. has agreed to settle hundreds of lawsuits over its defective hip replacements, the M2A Magnum. The law suits claim that the hip implants needed to be replaced ...
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Defective Hip Replacements: Stryker Agrees to Settle Suits

According to the Long Island News, Stryker has agreed to settle four New Jersey law suits related to defective hip replacements. The lawsuits involved the Stryker ABG II and Rejuvenate ...
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Defective Hip Replacements: Stryker and Biomet Suits Continue

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 ...
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Jury Awards $8.3M in Defective Hip Replacement Trial

In the first of nearly 11,000 DePuy defective hip replacement lawsuits to go to trial, a California jury found that Johnson & Johnson's DePuy division defectively designed its ASR hip ...
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Another J&J defective hip replacement recalled

Johnson & Johnson has alerted doctors in 21 countries to stop using their Adept hip implant, as the defective hip replacement has a higher than average failure rate.A British database ...
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First DePuy defective hip replacement trial underway

The first DePuy hip implant trial is underway in Los Angeles. In the case of Kransky v. DePuy, testimony has emerged that the DePuy ASR hip replacement system failed to ...
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FDA addresses defective medical devices

The U.S. Food and Drug Administration (FDA) proposed regulations restricting the sale of all-metal hip implants. Approximately 500,000 Americans have received these defective medical devices, many of which have failed ...
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Johnson & Johnson settles number of hip implant claims

According to Bloomberg News, Johnson & Johnson has agreed to settle the first three DePuy ASR defective hip replacement lawsuits for a sum of $600,000. Bloomberg reports that each of ...
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Stryker Orthopedics recalls hip implants

On July 6, 2012, Stryker Orthopedics announced that it was voluntarily recalling certain hip implant medical devices. According to the company's website, the recalled products are the Rejuvenate Modular and ...
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FDA investigating hip replacement medical device safety

The Food and Drug Administration (FDA) held a two-day meeting beginning on Wednesday, June 27th to study the safety of metal-on-metal hip replacement medical devices. The investigation was prompted by ...
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FDA to discuss defective hip replacements

In response to increasing reports of failure and adverse events, and concern over defective hip replacements, the U.S. Food and Drug Administration ("FDA") announced that it will hold a two-day ...
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Concerns mount over defective hip replacements

Recent studies have confirmed high rates of metal-on-metal hip replacement failures. In February 2011, the Food and Drug Administration issued a public health communication about these defective hip replacements. Instead ...
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