Events

Recall of HERMES POSTERIOR STABILIZED KNEE - TIBIAL PLATEAU

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by CERAVER - LES LABORATOIRES OSTEAL MEDICAL.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    40156
  • Event Risk Class
    II
  • Event Initiated Date
    2015-02-13
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    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.
  • Extra notes in the data
  • Reason
    Lors de la mise sous blisters de ces dispositifs en salle blanche avant le depart en sterilisation une inversion partielle s'est produite entre des pieces d'un lot de plateaux tibiaux hermes ps taille 4 epaisseur 9 et d'un lot de plateaux tibiaux hermed ps taille 5 epaisseur 9. des plateaux taille 5 sont presents dans les conditionnements etiquetes avec la reference des plateaux taille 4.

Device

HERMES POSTERIOR STABILIZED KNEE - TIBIAL PLATEAU

Manufacturer

CERAVER - LES LABORATOIRES OSTEAL MEDICAL
  • Manufacturer Address
    ROISSY
  • Manufacturer Parent Company (2017)
    Ceraver
  • Source
    HC