Stryker Hip Replacement Recall Lawyer:  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.


Recalled LFIT V40 Femoral Heads - Manufactured between 2002-2011
Catalog NumberImplant Head Diameter
6260-9-23636 mm
6260-9-24040 mm
6260-9-24444 mm
6260-9-34040 mm
6260-9-34444 mm
6260-9-44040 mm
6260-9-44444 mm









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:

  • Loss of mobility
  • ​Loss of range of motion
  • Pain 
  • Inflammation
  • Dislocation
  • Broken bones
  • Tissue damage  
  • Need for revision surgery

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:

  • Metallosis –  (harmful metal ions in the tissue, joint fluid, and blood)
  • Necrosis (premature tissue death)
  • Osteolysis (bone dissolution)
  • Pain and loosening of the hip implant
  • Pseudotumors – (resembles a tumor but is actually a mass of inflamed cells)
  • Need for revision surgery 


 History:

  • August 2016 - Stryker issued a product recall for its LFIT V40 Femoral Head component.
  • 2009, 2011 and 2013 – Stryker issued product recalls relating to packaging and manufacturing errors with its Accolade Hip Stem.
  • April 2012:  Stryker issues a “Urgent Safety Alert” for the Rejuvenate and ABG II systems listing excessive metal debris and/or ion generation as a safety risk to patients.

 
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

Telephone:  918-584-0070

Email:  CKG@CKGLawfirm.com

Mailing Address:
P.O. Box 1550
Jenks, OK  74037-1550


Physical Address:
406 S. Boulder Avenue, Suite 400
Tulsa, OK  74103-3800


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Accepting Cases from:
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Accepting Cases Nationwide  

​​​​​​​​​​​​​CYNTHIA K. GARRETT

Attorney at Law​

                                      

​​​​​​​​​​​Toll Free: ​866-584-0070

Accepting case throughout the United States, including these cities: Albuquerque, Atlanta, Arlington, Austin, Baltimore, Boston, Charlotte, Chicago, 
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STRYKER HIP REPLACEMENT RECALL LAWSUIT - LAWYER