CYNTHIA K. GARRETT
Attorney at Law
STRYKER HIP REPLACEMENT FAILURE
Currently accepting cases nationwide
The Stryker LFIT V40 Femoral Head was combined with other modular hip system components during hip replacement surgery. The femoral head locked into place at the junction of the head and stem. The femoral heads can corrode causing the locking function to fail.
If you received a hip replacement between 2002 and 2012, you may have a defective LFIT V40 femoral head.
Stryker Issues Urgent Medical Device Recall Notification To Medical Providers:
In August and September of 2016, Stryker issued an Urgent Medical Device Recall Notification to patients and doctors advising that the LFIT V40 femoral heads manufactured before 2011 had a higher than expected risk of taper lock failures. Stryker listed excessive metal debris as another potential risk.
LFIT V40 Femoral Heads are often found with Acccolade hip replacements.
|Catalog Number||Implant Head Diameter|
Other Defective Stryker Hip Replacement Products:
Rejuvenate – a recall was issued on April 2012.
ABG II - a recall was issued on April 2012.
Accolade – recalls were issued in 2009, 2011 and 2013 for packaging and manufacturing errors
Injuries Caused By Stryker Hip Replacement Failures:
The LFIT V40 femoral head taper lock connects the head to the femoral neck. When failure occurs the patient can experience:
The Stryker hip replacement products listed on this web page contain chromium, cobalt and titanium. Friction from normal movement, or the failure of the LFIT V40, can cause microscopic metal shavings to travel into surrounding tissues, joint fluid and blood stream. This can lead to a serious conditions including:
What To Do Now:
If you or a loved one: had a hip replacement since 2002 and have experienced any of the injuries or symptoms listed above, contact Cynthia K. Garrett, Attorney at Law, immediately to discuss your legal rights with an attorney.
Toll Free: 866-584-0070
P.O. Box 1550
Jenks, OK 74037-1550
406 S. Boulder Avenue, Suite 400
Tulsa, OK 74103-3800
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