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Stryker Issues Voluntary Recall Due To Defective Parts In Metal Hip Implant Devices

October 21st, 2016

Stryker Corporation is one of the leading manufacturers of metal hip implant devices. In the past, defective Stryker metal hip implants have caused serious injuries and adverse reactions in thousands of patients. In some cases, patients have even required revision surgery in order to remove and replace the defective Stryker hip implant parts.

Stryker recently issued a voluntary recall of all LFit V40 femoral heads manufactured between 2001 and 2011. Stryker LFit V40 femoral heads are prone to a high failure rate and pose potential risks to patient health and safety.  These defective hip components start to corrode. This can release harmful metal particles into the tissue and bloodstream surrounding the joint.

Government oversight agencies in both Canada and Australia have already issued safety warnings to doctors and patients about the high rate of failure among LFit V40 Femoral Head components. The Canadian government went as far as to issue an official recall of these components, sighting “higher than expected complaints of…failure.”

This is not the first time that a metal hip implant device manufactured by Stryker Corporation has been recalled due to safety concerns. In 2012, the FDA recalled all Stryker Rejuvenate and ABGII metal hip implant devices after patients complained that the devices failed and broke down at rates that were much higher than expected.

Stryker marketed their metal hip implant devices by promising patients and doctors increased durability and improved recovery times, compared to hip implant devices made from other manufacturers.

Unfortunately, once Patients that received a defective Stryker metal hip implant can experience painful and dangerous complications, including:

  • Osteolysis (bone dissolution)
  • Synovitis (inflammation of the synovial membrane)
  • Pseudo-tumors
  • Fluid in the joint
  • Tissue and bone necrosis
  • Metal poisoning in the blood
  • Revision surgery

If you or a loved one is experiencing any adverse reactions from Hip Replacement Surgery or if you have required painful Revision Hip Surgery, call The Yost Legal Group today at 1-800-YOST-LAW (967-8529).

When you call, one of our experienced Defective Medical Device attorneys will speak with you for FREE. The Yost Legal Group is made up of experienced attorneys ready to pursue your case with compassion and determination. We stand up to major medical device manufacturers on behalf of our clients and will fight hard to protect your rights.

The Yost Legal Group – Experienced Attorneys Dedicated to Protecting Your Rights

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