Events

Rappel de M/DN INTRAMEDULLARY FIXATION SYSTEM

Selon Health Canada (via FOI), ce/cet/cette rappel concerne un dispositif en/au/aux/à Canada qui a été fabriqué par ZIMMER BIOMET CANADA INC..

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    83890
  • Classe de risque de l'événement
    II
  • Date de mise en oeuvre de l'événement
    2017-05-03
  • Pays de l'événement
    Canada
  • Source de l'événement
    HC
  • Notes / Alertes
    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.
  • Notes supplémentaires dans les données
  • Cause
    Zimmer is initiating a field action for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures. specifically multiple test samples from each of the two configurations failed simulated distribution and shipping testing. the devices impacted are generally the heaviest outlier sizes within the respective product family.

Device

M/DN INTRAMEDULLARY FIXATION SYSTEM
  • Modèle / numéro de série
    Model Catalog: 00-2252-420-15 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-420-14 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-420-13 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-420-12 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-420-11 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-400-15 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-400-14 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-400-13 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-400-11 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-380-15 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-380-14 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-360-15 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-360-14 (Lot serial: ALL EXPIRING BEFORE MAY 2027); Model Catalog: 00-2252-340-16 (Lot serial: ALL EXPIRING BEFOR
  • Description du dispositif
    M/DN INTRAMEDULLARY FIXATION SYSTEM;VERSA FX FEMORAL FIXATION TUBE PLATES;ZIMMER NATURAL NAIL SYSTEM FEMORAL NAIL;ZIMMER NATURAL NAIL SYSTEM TIBIAL NAILS;ITST FEMORAL NAILS
  • Manufacturer
    ZIMMER BIOMET CANADA INC.

Manufacturer

ZIMMER BIOMET CANADA INC.
  • Adresse du fabricant
    MISSISSAUGA
  • Société-mère du fabricant (2017)
    Zimmer Biomet Holdings
  • Commentaire du fabricant
    “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