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
  • ID de l'événement
  • Classe de risque de l'événement
  • Date de mise en oeuvre de l'événement
  • Pays de l'événement
  • Source de l'événement
  • 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 of the nexgen pri femoral and provisional impactor/extractor (00-5901-026-00) and the replacement jaw assembly (00-5901-026-40) due to reports of spring clip fracture. instruments featuring an updated spring clip design introduced following a recall in march 2011 (#62540) have shown a similar failure rate. as a result zimmer has decided to discontinue these instruments.


  • Modèle / numéro de série
    Model Catalog: 00-5901-026-00 (Lot serial: 77000654); Model Catalog: 00-5901-026-40 (Lot serial: 77000574); Model Catalog: 00-5901-026-00 (Lot serial: 61800676); Model Catalog: 00-5901-026-40 (Lot serial: 77000573); Model Catalog: 00-5901-026-00 (Lot serial: 77000573); Model Catalog: 00-5901-026-40 (Lot serial: 61990656); Model Catalog: 00-5901-026-00 (Lot serial: 61990656); Model Catalog: 00-5901-026-40 (Lot serial: 61988272); Model Catalog: 00-5901-026-00 (Lot serial: 61988272); Model Catalog: 00-5901-026-40 (Lot serial: 61924920); Model Catalog: 00-5901-026-00 (Lot serial: 61924920); Model Catalog: 00-5901-026-40 (Lot serial: 61909414); Model Catalog: 00-5901-026-00 (Lot serial: 61909414); Model Catalog: 00-5901-026-40 (Lot serial: 61800676); Model Catalog: 00-5901-026-40 (Lot serial: 77000654); Model Catalog: 00-5901-026-00 (Lot serial: 61870067); Model Catalog: 00-5901-026-40 (Lot serial: 61870067); Model Catalog: 00-5901-026-00 (Lot serial: 62011774); Model Catalog: 00-5901-026-40 (Lot serial: 62011774
  • Description du dispositif
  • Manufacturer


  • Adresse du fabricant
  • Société-mère du fabricant (2017)
  • 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