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
    72045
  • Classe de risque de l'événement
    II
  • Date de mise en oeuvre de l'événement
    2017-06-08
  • 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 recall/removal for various 70cm guide wire trauma products which assist in guiding the nail during implantation. the humeral guide wire ball tip is also used to guide flexible reamers during ulna preparation for the nexel total elbow. the design verification for the previous packaging configuration does not cover the 70cm wires. while there have been no complaints involving a breach in sterility zimmer has completed design verification to move the 70cm guide wires to a new packaging configuration. as a result the products packaged in the previous packaging configuration are being removed.

Device

M/DN INTRAMEDULLARY FIXATION SYSTEM
  • Modèle / numéro de série
    Model Catalog: 00-2255-025-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 47-2490-098-00 (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 47-2255-008-00 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 47-2490-098-01 (Lot serial: >100 NUMBERS CONTACT MFR); Model Catalog: 00-2255-026-00 (Lot serial: >10 NUMBERS CONTACT MFR)
  • Description du dispositif
    M/DN INTRAMEDULLARY FIXATION HUMERAL GUIDE WIRE;ZIMMER NATURAL NAIL SYSTEM TEAR DROP GUIDE WIRE;HUMERAL GUIDE WIRE BALL TIP
  • 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