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Stryker Hip Recall | StRyker Hip Revision Lawyers | Stryker Hip Implant Lawsuits

Stryker LFIT V40 CoCr Anatomic Femoral Head recall

More than 100,000 LFIT V40 CoCr Anatomic Femoral Head devices have been implanted into patients. On August 29, 2016, Stryker Corporation issued an urgent medical device recall on this product. The Stryker LFIT V 40 Anatomic Femoral Head represents one part of a replacement hip. It is used in many hip replacement hip stems manufactured and marketed by Stryker.

In the recall letter, Stryker outlined the reported problems associated with the device:
• Insufficient range of motion
• Loss of implant/bone fixation strength
• Excessive wear debris
• Noise
• Dislocation of the femoral head from the hip stem
• Hip stem fractures
• Excessive metallic corrosion leading to cobalt and/or chromium poisoning.

Stryker Corporation has now been sued over this device with lawsuits pending in three different jurisdictions. A plaintiff has requested that the Judicial Panel on Multidistrict Litigation (JPMDL) consolidate litigation against Stryker. The plaintiff proposed that the new MDL be located in federal court in Massachusetts. contends that Stryker knew for years that the LFIT V 40 femoral heads were defective and dangerous. However they failed to properly warn the physicians implanting these devices and ignored the risks to patients.

If you were implanted with a metal on metal hip and suffered complications as a result, please contact for a free consultation.

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Stryker rejuvenate, abg II & Accolade metal hip implant recalls

The Stryker metal hip recall lawyers at are also currently handling claims involving the following Stryker hip replacements:

- Stryker Rejuvenate
- Stryker ABG II
- Stryker Accolade

The most common hip implants include a one-piece neck and stem called a ‘monoblock’ design. Stryker’s Rejuvenate and ABG II systems include several neck and stem components.  It is our opinion that the design and manufacture of these components was grossly defective.

Stryker Hip RECALL - Stem Complications

Recent recalls of hip implants (such as those manufactured by DePuy and Biomet) have focused on the metal-on-metal ball-and-socket components, which can release metallic debris into the body during normal wear and tear.

Stryker’s modular-neck hip stem systems are different.

However, because the Stryker necks are made of chromium and cobalt, and the stems are coated with titanium, they do have a metal-on-metal junction. And they can cause the same complications as other defective hip implants.

Several recalls and “Safety Alerts” have issued concerning these Stryker components.  One of the official alerts listed the potential hazards in these devices, including: “Excessive metal debris and/or ion generation,” caused by “fretting and/or corrosion at or about the modular neck junction,” which “may lead to increased metal ion generation in the surrounding joint space.”

The safety of metal-on-metal hip devices is seriously in issue because of the tendency for metal components to rub against one another, depositing minute shards of metal into a patient’s tissues, bones or bloodstream.

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Complications associated with recalled Stryker metal hip implants often lead to complex revision (removal) surgery and include:

Stryker hip attorneys at are handling cases for patients with Stryker Rejuvenate, Stryker ABG II and Stryker Accolade who have suffered from any of the above symptoms. 

**Updated Information**

Stryker has begun settling some of the lawsuits. Each person who underwent a qualified revision surgery was entitled to a base payment of $300,000. For patients with bilateral revised implants, the base award was $600,000. These base awards are the highest of any hip settlement to date.

There are two important limits on calculating the amount of compensation you may receive however. First, these base awards were subject to limited deductions. For example, the amount was reduced for patients over 70 up to 20%. There were no reductions to this base payment for obesity, smoking, diabetes or other factors commonly seen in other hip implant settlements.

Second, because compensation is based on individual injury, how much compensation each individual can expect will depend solely upon his or her own circumstances while experiencing complications related to their Stryker hip.

Stryker hip claims lawyers at have been handling defective medical device cases for over 16 years, and have successfully handled cases including, Fen/phen, Guidant defibrillator, Vioxx, Medtronic Lead wire, Prempro, and pelvic mesh. 

Let us put our years of experience to work helping you and your family.

If you or a loved one has suffered any symptoms after receiving a metal hip implant, you may be entitled to compensation. Our award-winning lawyers have set records in settlements and trials for obtaining fair compensation for our clients and can file a lawsuit on your behalf. Call now to speak with an experienced legal professional for free.

Click for important information about Bair Hugger Blanket Infections used after surgery!

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