Events

Recall of AIRWAY CONNECTION SYSTEM

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH.

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
    32012
  • Event Risk Class
    II
  • Event Initiated Date
    1999-07-13
  • 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
    Defectuosite trouvee dans la mesure de o2 cause par un eprom u42 qui n'indiquerait pas une erreur du zero de o2 si le capteur de o2 devient defectueux. pourrait afficher mesures de o2 erronees.

Device

AIRWAY CONNECTION SYSTEM

Manufacturer

PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH
  • Manufacturer Address
    BOEBLINGEN
  • Source
    HC