On September 27, 2016, Australian health authorities issued a “Hazard Alert” over the risk of injuries relating to the Stryker LFIT V40 femoral head hip implant components citing the same dangers and warning consumers and health professionals about the higher than expected incidence of failures and injuries relating to Stryker LFIT V40 hip implant components. Specific item numbers of the affected models are listed below.
Previously, on August 29, 2016, Stryker Corporation issued a recall for the LFIT V40 series of femoral heads manufactured before 2011. These heads are often used with the Accolade stem and are showing a high incidence of failures leading to patient injuries including loss of mobility; pain; inflammation; adverse local tissue reaction; dislocation; joint instability; broken bones around the components; leg length discrepancy; and a need for complicated and painful revision surgery. Specific health hazards associated with the issues include disassociation of the femoral head from the hip stem; implant fractures; increased metallic debris in the body; insufficient range of movement; insufficient tissue tension; increased wear debris, and total loss of implant.
Contact National Hip Implant Failure Injury Lawyers
If you or a family member have experienced problems with a Stryker LFIT V40 femoral head hip implant, or have been told your implant should be replaced, please use the form on this page right now to contact an experienced Lieff Cabraser personal injury lawyer about your case. Or you may call us toll-free at 1 800-541-7358 and ask to speak to attorney Lexi J. Hazam. You can also visit our Stryker LFIT V40 case page for more information. There is no charge or obligation of any kind for our review of your Stryker Anatomic hip injury case.
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