Recall Or Safety Alert for AutoSet CS, AutoSet CS PaceWave, AutoSet CS2, AutoSet CS-A, VPAP Adapt, VPAP Adapt SV, VPAP Adapt SV-A, VPAP Tx, S9 AutoSet CS, S9 AutoSet CS PaceWave, S9 AutoSet CS-A , S9 AutoSet CS-A PaceWave, S9 VPAP ADAPT, S9 VPAP Adapt eASV, S9 VPAP Adapt PaceWave, S9 VPAP Tx, AirCurve 10 ASV, AirCurve 10 CS PaceWave, Lumis Tx

According to Austrian Federal Office for Safety in Health Care (BASG), this recall or safety alert involved a device in Austria that was produced by ResMed Ltd.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Recall / Safety alert
  • Date
    2015-05-27
  • Event Country
  • Event Source
    BASG
  • Event Source URL
  • Notes / Alerts
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Extra notes in the data

Manufacturer