Retiro De Equipo (Recall) de Device Recall ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por Stryker Howmedica Osteonics Corp..

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
  • ID del evento
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
  • Fecha de inicio del evento
  • Fecha de publicación del evento
  • Estado del evento
  • País del evento
  • Fecha de finalización del evento
  • Fuente del evento
  • URL de la fuente del evento
  • Notas / Alertas
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notas adicionales en la data
    Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate - Product Code MEH
  • Causa
    Product deviation : specific lots of sprayed ha hip stems did not meet stryker's internal material specification for tensile bond strength and crystallinity.
  • Acción
    An "Urgent Product Recall" letter was sent via Federal Express on January 6, 2009 with return receipt to Stryker Branches/Agencies, Hospital Risk Management, Hospital Chief of Orthopaedics and Surgeons. The letter described the affected product, issue, potential hazards and risks. Stryker Branches and Hospital Risk Management were asked to examine their inventory for affected product. Stryker Representatives were instructed to contact customers to reconcile and return recalled product to Stryker Orthopaedics. All letters include a response form to be completed and returned indicating that they have been informed of the recall and the amount of product on hand, if any. Direct questions about the recall to Stryker Orthopaedics at 1-201-831-5718.


  • Modelo / Serial
    6021-3535 ACCOLADE (127 DEG) SIZE 3.5 24956202 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25025001 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25025003 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25025004 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25046901 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25080901 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25080902 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25095701 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25169903 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25190601 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25212102 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25232001 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25243801 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25256201 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25275701 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25275702 and 6021-3535 ACCOLADE (127 DEG) SIZE 3.5 25275703.
  • Clasificación del producto
  • Clase de dispositivo
  • ¿Implante?
  • Distribución
    Nationwide Distribution.
  • Descripción del producto
    Accolade TMZF Plus Hip Stem; Hydroxylapatite coated, Titanium Plasma Spray; || V40 taper || Longitudinal Grooves, Stem Length 120mm, Head Offset - 43mm, 127 degree neck angle. || Hip stems are single use devices intended for cementless fixation. The products are intended for use in primary reconstruction of the proximal femur or revision of a previous total hip arthroplasty.
  • Manufacturer


  • Dirección del fabricante
    Stryker Howmedica Osteonics Corp., 325 Corporate Dr, Mahwah NJ 07430
  • Empresa matriz del fabricante (2017)
  • Source