Device Recall Reflection Interfit Shell, 52 MM OD, 3 HOLE

  • Modelo / Serial
    Batch No. 13EM03053
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    Worldwide Distribution: US Distribution to NJ and FL; and the countries of: Colombia and Costa Rica.
  • Descripción del producto
    Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc. || Indications for use include cemented or uncemented total hip arthroplasty for rheumatoid arthritis; osteoarthritis; post traumatic arthritis, avascular necrosis; femoral and neck fractures; osteomyelitis; fracture, dislocation of the hip; and unsuccessful cup arthroplasty, endoprosthesis, femoral osteotomy, or girdlestone resection.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Smith & Nephew Inc, 1450 E. Brooks Rd, Memphis TN 38116
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA