Federal MDL Created for Stryker LFIT Anatomic CoCR V40 Prosthetic Hip in the District of Massachusetts Before Judge Indira Talwani

Federal MDL Created for Stryker LFIT Anatomic CoCR V40 Prosthetic Hip

LFIT V40 Femoral Head Recall

The Judicial Panel on Multidistrict Litigation (JPMDL) has created new MDL No. 2768 to hear products liability litigation involving the Stryker-branded LFIT Anatomic CoCR V40 femoral heads, a prosthetic hip replacement device. [Read more…]

Stryker LFIT V40 Femoral Head Hip Implant Recall

Stryker LFIT V40 Femoral Head Hip Implant Recall

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. [Read more…]