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How can a Stryker Implant Fail and how can its Failure Hurt Me?

  • Corrosion at the neck/stem junction causes failure of modular implants
  • Corrosion releases potentially toxic heavy metal ions into the soft tissues and bone surrounding the hip
  • If untreated, heavy metal ions invade the blood stream and can cause systemic heavy metal toxicity
  • Local and systemic heavy metal toxicity have been linked to tissue and bone death as well as organ failure and ultimately device removal
  • The only available treatment is to remove the entire device
  • Significant risks are associated with device removal surgery including:
    • Infection
    • Unintended bone fracture
    • Removal of large sections of necrotic tissue
    • Significantly increased risk of dislocation
    • Leg length discrepancy
    • Pain from the larger replacement hip implant
    • Extended rehabilitation

The “Stryker Rejuvenate” system:

  • Released by Stryker in February of 2010
  • Is a modular system designed to re-create a patient’s natural anatomy
  • Is designed to promote easier installation with varieties of component designs
  • Necks composed of heavy metal cobalt and chromium
  • Stems with a titanium coating on the stem

Hip implants like the “Rejuvenate” system and the ABG II are used for correcting joint failure caused by a variety of conditions like osteoarthritis. The indications for the total hip replacement are:

  • Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis;
  • Rheumatoid arthritis;
  • Correction of functional deformity;
  • Revision procedures where other treatments or devices have failed;
  • Treatment of nonunion, femoral neck and trochanteric fractures of the proximal femur with head involvement that is unmanageable using other techniques.

Call us today. We charge no fee or costs unless we make a recovery for you. Call us day or night at 800-862-1260.

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