Events

Retiro De Equipo (Recall) de ANATOMICAL SHOULDER INVERSE/REVERSE - HUMERAL PE-INLAY

Según Health Canada (via FOI), este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Canada que fue producido por ZIMMER BIOMET CANADA INC..

¿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
    53643
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    2012-08-08
  • 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
    Zimmer is initiating this product safety corrective action to inform customers with consignment product to check patient labels against product labels during the surgery for some products manufactured by the zimmer gmbh production site in winterthur (switzerland) before march 2010. in rare cases product information on the patient label with respect to ref number and lot number might not coincide with the corresponding information on the product label (which is correct).

Device

ANATOMICAL SHOULDER INVERSE/REVERSE - HUMERAL PE-INLAY
  • Modelo / Serial
    Model Catalog: 01.04223.406 (Lot serial: CONTACT MFR); Model Catalog: 01.04223.366 (Lot serial: CONTACT MFR); Model Catalog: 01.04223.360 (Lot serial: CONTACT MFR); Model Catalog: 01.04214.405 (Lot serial: CONTACT MFR); Model Catalog: 01.04214.345 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.020 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.017 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.016 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.015 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.013 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.012 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.011 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.010 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.009 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.008 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.007 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.006 (Lot serial: CONTACT MFR); Model Catalog: 01.00295.005 (Lot serial: CONTACT MFR); Model Catalog: 01-00351.265 (Lot
  • Descripción del producto
    ANATOMICAL SHOULDER INVERSE HUMERAL PE
  • Manufacturer
    ZIMMER BIOMET CANADA INC.

Manufacturer

ZIMMER BIOMET CANADA INC.
  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
    Zimmer Biomet Holdings
  • 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
    HC