Events

Rappel de NEXGEN COMPLETE KNEE SOLUTION POROUS PATELLA DRILL GUIDE

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
    51241
  • Classe de risque de l'événement
    II
  • Date de mise en oeuvre de l'événement
    2013-11-22
  • 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
    Since the march 2012 notification zimmer has monitored the occurrence of non-compatible micro component combinations being implanted. this included the usage of micro femurs and micro patellae in addition to micro articular surfaces. although the occurrence has been reduced since the 2012 notification it has not been eliminated and therefore zimmer is initiating a recall to remove the affected devices [implants and provisionals (a reusable joint specific trial device used in orthopedic joint replacement to validate the proper size of the permanent prosthesis)] and prevent this issue from recurring.

Device

NEXGEN COMPLETE KNEE SOLUTION POROUS PATELLA DRILL GUIDE
  • Modèle / numéro de série
    Model Catalog: 00-5879-067-29 (Lot serial: ALL LOTS); Model Catalog: 00-5879-067-26 (Lot serial: ALL LOTS); Model Catalog: 00-5878-061-26 (Lot serial: ALL LOTS); Model Catalog: 00-5878-061-29 (Lot serial: ALL LOTS); Model Catalog: 00-5878-061-32 (Lot serial: ALL LOTS); Model Catalog: 00-5878-061-35 (Lot serial: ALL LOTS); Model Catalog: 00587906126 (Lot serial: ALL LOTS); Model Catalog: 00587906129 (Lot serial: ALL LOTS); Model Catalog: 00587906132 (Lot serial: ALL LOTS); Model Catalog: 00587906135 (Lot serial: ALL LOTS)
  • Description du dispositif
    NEXGEN COMPLETE KNEE SOLUTION POROUS PATELLA DRILL GUIDE
  • 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