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Stryker Howmedica Osteonics Corp. recalls Special Orthopaedic Solution Peri-Acetabular Prosthesis V40 Femoral Extension Component Product Usage: The PAR ex
Recalled November 21, 2012 · FDA recall Z-0286-2013 · Stryker Howmedica Osteonics
Hazard
Stryker has become aware that insufficient taper torsional strength may result when a PAR extension piece is used with a forged CoCr stem. · FDA Class II
Units
301 units
Sold at
Worldwide Distribution - US Nationwide
Description
Stryker has become aware that insufficient taper torsional strength may result when a PAR extension piece is used with a forged CoCr stem.
Product
Special Orthopaedic Solution Peri-Acetabular Prosthesis V40 Femoral Extension Component Product Usage: The PAR extension piece is a component of the PAR assembly. The Peri-Acetabular Reconstruction (PAR) endoprosthesis was developed to meet the unique needs of patients who require reconstruction of large acetabular defects after a Type I and II pelvic resection.
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →