Device Recall Hipstar V40 Femoral Stem

  • Model / Serial
    Catalog # Lot Code 78501006 G1167520 78501006 G1167521 78501006 G1167521 78501006 G1228787 78501006 G1229912 78501006 G1229912 78501006 G1230461 78501006 G1230461 78501006 G1239108 78501006 G1239108 78501007 G1229913 78501008 G1214896 78501008 G1214896 78501008 G1214896 78501008 G1214896 78501008 G1214896 78501009 G1076126 78501009 G1076126 78501009 G1076126 78501009 G1090547 78501009 G1090547 78501009 G1090547 78501009 G1090547 78501009 G1230631 78501009 G1230631 78501010 G1167526 78501010 G1167526 78501010 G1214894 78501010 G1214894 78501010 G1214894 78501010 G1214894 78501010 G1214894 78501010 G1285646 78501010 G1285646 78501011 GC981487 78501011 GC981487 78501011 GC981487 78501011 GC981487 78501011 GC981487 and 78501012 GC966512
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide
  • Product Description
    Hipstar V40 Femoral Stem || Howemedica: || Benoist Girard et Cie; 203 bd de la Grande Selle B.P.8; 14201 Herouville Saint Clair. Used in total and hemi hip arthroplasty for: noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis; Rheumatoid arthritis; Correction of functional deformity; revision procedures where other treatments or devices have failed; and treatment of nonunion, femoral neck and trochanteric fractures of the proximal femur with head involvement that are unmanageable using other techniques.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Stryker Howmedica Osteonics Corp., 325 Corporate Dr, Mahwah NJ 07430
  • Manufacturer Parent Company (2017)
  • Source
    USFDA