Events

Retiro De Equipo (Recall) de PATIENT PROGRAMMER (97740)

Según Health Canada (via FOI), este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Canada que fue producido por MEDTRONIC OF CANADA 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
    20946
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    2014-02-13
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
  • Causa
    Purpose of this recall is to inform about changes to the adverse event labeling for medtronic spinal cord stimulation therapy. the issue is the potential for patients to experience spinal cord compression weeks to years after implant of spinal cord stimulation (scs) lead. spinal cord compression can lead to neurological deficit due to the formation of reactive fibrous tissue sometimes with an inflammatory component. the time to onset for spinal cord compression ranges from weeks to over 17 years and may progress after lead removal.

Device

PATIENT PROGRAMMER (97740)
  • Modelo / Serial
    Model Catalog: 97740 (Lot serial: All Lots); Model Catalog: 37712 (Lot serial: All Lots); Model Catalog: 37744 (Lot serial: All Lots); Model Catalog: 37702 (Lot serial: All Lots); Model Catalog: 39565 (Lot serial: All Lots); Model Catalog: 7427 (Lot serial: All Lots); Model Catalog: 37704 (Lot serial: All Lots); Model Catalog: 37711 (Lot serial: All Lots); Model Catalog: 37703 (Lot serial: All Lots); Model Catalog: 3587A (Lot serial: All Lots); Model Catalog: 97714 (Lot serial: All Lots); Model Catalog: 3986A (Lot serial: All Lots); Model Catalog: 37714 (Lot serial: All Lots); Model Catalog: 977D260 (Lot serial: All Lots); Model Catalog: 977D160 (Lot serial: All Lots); Model Catalog: 977A160 (Lot serial: All Lots); Model Catalog: 977A275 (Lot serial: All Lots); Model Catalog: 977A260 (Lot serial: All Lots); Model Catalog: 977A190 (Lot serial: All Lots); Model Catalog: 977A175 (Lot serial: All Lots); Model Catalog: 977A290 (Lot serial: All Lots); Model Catalog: 7427V (Lot serial: All Lots); Model Catalog: 977
  • Descripción del producto
    PATIENT PROGRAMMER (97740)
  • Manufacturer
    MEDTRONIC OF CANADA LTD.

Manufacturer

MEDTRONIC OF CANADA LTD.
  • Dirección del fabricante
    BRAMPTON
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    HC