Events

Retiro De Equipo (Recall) de LEVEEN INFLATOR

Según Health Canada (via FOI), este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Canada que fue producido por BOSTON SCIENTIFIC 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
    28133
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    2001-06-25
  • 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
    A hole in a small quantity of trays was discovered that may compromise the product sterility.

Device

LEVEEN INFLATOR
  • Modelo / Serial
    Model Catalog: 710-112 (Lot serial: BATCH #S: 2661794 1751033); Model Catalog: 710-112 (Lot serial: 2780327 2891101 3246930); Model Catalog: 710-112 (Lot serial: 2432778 2029900 2029899); Model Catalog: 710-112 (Lot serial: 2635009 3153775 3384516); Model Catalog: 710-112 (Lot serial: 2916051 3108638 3153775); Model Catalog: 710-112 (Lot serial: 1705906 1751033 1805211.); Model Catalog: 710-112 (Lot serial: 3349455 2840951 1856697)
  • Descripción del producto
    LEVEEN INFLATOR WITH PRESSURE GAUGE 20
  • Manufacturer
    BOSTON SCIENTIFIC LTD.

Manufacturer

BOSTON SCIENTIFIC LTD.
  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
    Boston Scientific
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    HC