Events

Recall Or Safety Alert for Patient monitor, Fetal monitor, B-Ultrasound Diagnosis system, Puls-Oxymeter, Electrocardiograph, Pocket Fetal Doppler, Visual Elextronic Stethoscope, Multifunctional Visual Stethoscope, Dynamic ECG-system, Digital Brain Electric Activity Mapping, Syringe pump, Infusion pump

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 ARI Technology (Group) Co., 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
    2013-06-27
  • Event Country
    Austria
  • Event Source
    BASG
  • Event Source URL
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • 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

Device

Patient monitor, Fetal monitor, B-Ultrasound Diagnosis system, Puls-Oxymeter, Electrocardiograph,...

Manufacturer

ARI Technology (Group) Co., Ltd.
  • Source
    AFOSHCBASG