Events

Rappel de EOPS OCULOPLASTIC MSH-LF

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

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
    47210
  • Classe de risque de l'événement
    II
  • Date de mise en oeuvre de l'événement
    2017-03-09
  • 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
    Medline industries received a recall notice from medtronic concerning the covidien curity eye pad oval. medtronic has identified several lots of the eye pad oval where the sterile packaging may be compromised. the eye pad oval is a component in some medline custom or procedure packs. medline is therefore issuing a recall for the packs containing the eye pad.

Device

EOPS OCULOPLASTIC MSH-LF
  • Modèle / numéro de série
    Model Catalog: DYNJ48515X (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: DYNJ48518X (Lot serial: 14XB0993); Model Catalog: DYNJ48518X (Lot serial: 15EB6801); Model Catalog: DYNJ48518X (Lot serial: 15HB6030); Model Catalog: DYNJ48518X (Lot serial: 15VB3988); Model Catalog: DYNJ48518X (Lot serial: 15XB3841); Model Catalog: DYNJ48518X (Lot serial: 168B1087); Model Catalog: DYNJ48518X (Lot serial: 16OB9796); Model Catalog: DYNJ48518X (Lot serial: 16QB5514); Model Catalog: DYNJ48518X (Lot serial: 16WB4888); Model Catalog: DYNJ48518X (Lot serial: 17MB3958); Model Catalog: DYNJ48513X (Lot serial: 16GB5019); Model Catalog: DYNJ48513X (Lot serial: 15AB2357); Model Catalog: DYNJ48513X (Lot serial: 15BB5058); Model Catalog: DYNJ48513X (Lot serial: 15CB5721); Model Catalog: DYNJ48513X (Lot serial: 15VB1678); Model Catalog: DYNJ48513X (Lot serial: 16CB5775); Model Catalog: DYNJ48513X (Lot serial: 16LB8222); Model Catalog: DYNJ48513X (Lot serial: 17CB0873); Model Catalog: DYNJ47475X (Lot serial: 17AB1354); Model Ca
  • Description du dispositif
    EOPS OCULOPLASTIC MSH-LF;EXTERNAL DCR MSH-LF;ENDONASAL DCR MSH-LF;CATARACT PACK
  • Manufacturer
    MEDLINE CANADA CORPORATION

Manufacturer

MEDLINE CANADA CORPORATION