Retiro De Equipo (Recall) de Vanguard 360 Femoral Boss Reamer

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Biomet Australia Pty Ltd.

¿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
    Recall
  • ID del evento
    RC-2014-RN-00907-1
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
    2014-08-18
  • País del evento
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
  • Notas / Alertas
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • Notas adicionales en la data
  • Causa
    Biomet has initiated this action following an investigation which identified that the vanguard 360 femoral boss reamer may not fit into the mating component. this issue may result in delay to surgery while an unaffected reamer is sourced. it is likely that this issue will be identified prior to the surgical procedure. there have been no reports of patient injury related to this issue.
  • Acción
    Hospitals are requested to immediately locate and discontinue use of the product and its return to Biomet. This action has been closed-out on 03/06/2016.

Device

  • Modelo / Serial
    Vanguard 360 Femoral Boss ReamerPart number: 32-488474 Lot numbers: 095780, 308620, 418970, 708240, 726490, 953540ARTG number: 116459
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    DHTGA