Events

Rappel de ZMR HIP SYSTEM - FEMORAL STEMS - POROUS STEMS

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
    147422
  • Classe de risque de l'événement
    I
  • Date de mise en oeuvre de l'événement
    2011-10-27
  • 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
    This action is being conducted for a labeling correction of the zmr porous revision hip prosthesis and zmr revision taper hip prosthesis including the indications for use contraindications and warnings. investigation has shown the potential for fracture of the zmr revision hip system where bone quality and bone quantity (especially in the proximal location) and resultant proximal support is not optimal. the device indication will now be limited to cementless revision hip arthroplasty.

Device

ZMR HIP SYSTEM - FEMORAL STEMS - POROUS STEMS
  • Modèle / numéro de série
    Model Catalog: 00-9981-225-22 (Lot serial: ALL LOTS); Model Catalog: 00-9981-210-32 (Lot serial: ALL LOTS); Model Catalog: 00-9981-210-22 (Lot serial: ALL LOTS); Model Catalog: 00-9983-240-33 (Lot serial: ALL LOTS); Model Catalog: 00-9983-240-32 (Lot serial: ALL LOTS); Model Catalog: 00-9983-225-34 (Lot serial: ALL LOTS); Model Catalog: 00-9983-225-33 (Lot serial: ALL LOTS); Model Catalog: 00-9983-225-32 (Lot serial: ALL LOTS); Model Catalog: 00-9983-210-34 (Lot serial: ALL LOTS); Model Catalog: 00-9983-210-33 (Lot serial: ALL LOTS); Model Catalog: 00-9983-210-32 (Lot serial: ALL LOTS); Model Catalog: 00-9983-195-34 (Lot serial: ALL LOTS); Model Catalog: 00-9983-195-33 (Lot serial: ALL LOTS); Model Catalog: 00-9983-195-32 (Lot serial: ALL LOTS); Model Catalog: 00-9983-180-34 (Lot serial: ALL LOTS); Model Catalog: 00-9983-180-33 (Lot serial: ALL LOTS); Model Catalog: 00-9983-180-32 (Lot serial: ALL LOTS); Model Catalog: 00-9983-165-34 (Lot serial: ALL LOTS); Model Catalog: 00-9983-165-33 (Lot serial: ALL LOTS
  • Description du dispositif
    ZMR HIP SYSTEM POROUS STEMS LINE EXT.
  • 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