Stryker Accolade Hip Replacement Case Evaluation

Serious problems with Stryker Accolade hip replacements have been reported by individuals nationwide, including cases where the hip stem frets and corrodes, which may result in premature hip failure, loosening, pain, and other complications that may result in the need for hip revision surgery.

The lawyers at Saiontz & Kirk, P.A. are reviewing potential Stryker Accolade hip lawsuits for individuals who may have experienced problems related to the use of an LFIT Anatomic V40 Femoral Head or other components that may be unreasonable dangerous and defective.

Contact Our Lawyers to Review aSTRYKER HIP CASE

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Saiontz & Kirk, PA, Attorneys & Lawyers, Baltimore, MD

Financial compensation and settlements are being pursued for individuals who received a Stryker Accolade hip implant, and experienced complications like:

  • Hip Implant Loosening, Failure or Disassociation with the Femoral Head
  • Pain, Discomfort and Loss of Mobility
  • Metal Blood Poisoning
  • The Need For Artificial Hip Revision Surgery

All claims are handled by our law firm on a contingency fee basis, so there are never any costs or attorney fees unless a recovery is obtained. Request a free consultation and claim evaluation.

Stryker Accolade Hip Problems

The Stryker Accolade TMZF hip stem was first introduced in March 2000, consisting of a single piece of titanium that is implanted into the patient’s femur. Stryker stopped producing the original Accolade in 2012, and replaced it with the Accolade II, which is manufactured from a different type of titanium.

The change came following reports that the hip stem could fret and corrode, shedding chromium and cobalt debris into the surrounding tissue. This can cause a condition known as metallosis, or metal hip poisoning, which may lead to the death of the surrounding tissue and high levels of metal in the blood. It can also result in the corroded stem failing.

Stryker Accolade hip complications could also be caused by the use of certain Stryker LFit V40 femoral head components manufactured before 2011.

In August 2016, Stryker issued an urgent field action notice (PDF) to orthopedic surgeons worldwide, warning about the LFit V40 femoral head, which is commonly used with Stryker Accolade hip replacements.

The Stryker LFit V40 Femoral Head has been linked to a higher than usual rate of failures, resulting in pain, loss of mobility, the shedding of metal debris, and often the need for revision surgery.

Stryker Accolade Class Action Lawyers

Financial compensation may be available through a Stryker Accolade or Stryker LFit V40 lawsuit due to the unreasonably dangerous and defective design associated with certain devices.

While many individuals are unaware of the specific components used during their orthopedic surgery, the Stryker hip lawyers at Saiontz & Kirk, P.A. provide free consultations and case evaluations for individuals nationwide.

Contact our law firm today if you or a loved one:

  • Have Been Notified About Problems with Your Hip Replacement
  • Have Received Cobalt and Chromium Blood Testing
  • Required Revision Surgery for Problems with a Stryker Hip Replacement