Retiro De Equipo (Recall) de BVM (Bag-Valve-Mask) Manual Resuscitation Systems

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

¿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 I
  • Fecha de inicio del evento
  • País del evento
  • Fuente del evento
  • 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
    Medical developments international has identified the possibility that the valve of the bvm manual resuscitation system may become stuck during storage. this could result in the intended tidal volume not being delivered through the valve, which may cause a delay in treatment.The instructions for use (ifu) provided with these products include the requirement to ensure the bag, valve and oxygen delivery is functioning correctly prior to use.
  • Acción
    Medical Developments International is requesting users inspect their stocks and quarantine all units from the affected batch numbers, then complete the supplied Reply Form and email or fax it back so that we may arrange collection and issue credit. Please complete the Reply Form even if you have no stock which is subject to recall, as we require this information to reconcile the process.


  • Modelo / Serial
    BVM (Bag-Valve-Mask) Manual Resuscitation SystemsCatalogue Number: RS-7595-BVMDAWBatch Numbers: up to 1170328006Catalogue Number: RS-7595-BVMDABatch Numbers: up to 1160629050Catalogue Numbers: RS-7595-BVMDC, RS-7595-BVMDC3Batch Numbers: up to 1160728029Catalogue Number: RS-7595-BVMDC3Batch Numbers: up to 11600922002ARTG Number: 147543
  • Manufacturer