Devices

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
Orthopedic Devices
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
Stryker Howmedica Osteonics Corp.
1 Event
- Recall of Device Recall Hipstar V40 Femoral Stem

Manufacturer

Stryker Howmedica Osteonics Corp.

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

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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