Retiro De Equipo (Recall) de MAQUET HLS and PLS Sets with BIOLINE Coating (extracorporeal support sets)BE-HLS 5050 HLS Set Advanced 5.0

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Maquet 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-2016-RN-01514-1
  • Clase de Riesgo del Evento
    Class I
  • Fecha de inicio del evento
    2016-11-17
  • 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
    In january 2015 maquet cardiopulmonary noticed an increase in the frequency of complaints for the hls and pls sets regarding blood leaking from the gas outlet connector. in the defective products between 6-14 fibers have separated from the polyurethane casting (or 'potting'), which is at the ends of the fibers. this separation allows patient blood to leak out of the system (via the gas outlet connector). a safety alert was issued to alert customers regarding this issue at the time.Since the release of safety alert, maquet has identified the root cause and have implemented and validated the necessary corrections that return the products to their original performance specifications. due to the risks associated with the use of the oxygenators with increased leakage, maquet is now initiating a recall of the potentially affected lot numbers.
  • Acción
    Customers are advised to quarantine affected products in their inventory and return them to Maquet. A credit will be issued upon receipt of the returned products.

Device

  • Modelo / Serial
    MAQUET HLS and PLS Sets with BIOLINE Coating (extracorporeal support sets)BE-HLS 5050 HLS Set Advanced 5.0 Product Order Number: 70104.8127All Lot Numbers below 70104520BE-HLS 7050 HLS Set Advanced 7.0 Product Order Number: 70104.7753All Lot Numbers below 70100115BE-PLS 2050 PLS SetProduct Order Number: 70102.7818All Lot Numbers below 70104119BE-PLS 2051 PLS Set PlusProduct Order Number: 70105.0310All Lot Numbers below 70102843ARTG Numbers: 193475, 192105
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    DHTGA