Stryker LFIT V40 Femoral Head Hip Implant
Clark, Perdue & List is investigating injury claims related to failure of the Stryker LFIT V40 Femoral Head Hip Implant
Stryker LFIT V40 Femoral Head Hip Implant is used in hip replacement surgeries. According the the Australian equivalent of the FDA in the United States, the Stryker LFIT has “a higher than expected incidence of taper lock failures.”
The Stryker hip implant system features three components. The femoral neck is inserted into the thigh bone. The femoral head is the ball which rotates inside the hip socket. The taper lock connects the femoral neck to the femoral head. Failure of the taper lock could cause severe complications, including the need for additional surgery.
Our unsafe medical device lawyers are investigating potential claims of patients who were implanted with the Stryker LFIT V40 Femoral Head hip implant and who have suffered complications. Contact us for a free consultation.
If you or a loved one has been harmed by a unsafe medical device, contact us for a free consultation.
More About Unsafe Medical Devices
BLOG POSTS ABOUT DEFECTIVE HIP REPLACEMENTS
Stryker LFIT V40 Femoral Head Recall
Read More
Stryker hip implant settlement announced
Read More
Stryker Defective Hip Replacements Bellwether Trials Set
Read More
Defective Hip Replacements: Biomet Agrees to Settlements
Read More
Defective Hip Replacements: Stryker Agrees to Settle Suits
Read More
Defective Hip Replacements: Stryker and Biomet Suits Continue
Read More
Jury Awards $8.3M in Defective Hip Replacement Trial
Read More
Another J&J defective hip replacement recalled
Read More
First DePuy defective hip replacement trial underway
Read More
FDA addresses defective medical devices
Read More
Johnson & Johnson settles number of hip implant claims
Read More
Stryker Orthopedics recalls hip implants
Read More
FDA investigating hip replacement medical device safety
Read More
FDA to discuss defective hip replacements
Read More
Concerns mount over defective hip replacements
Read More