Events

Safety Alert for Trilogy 100, 200 and 202 Ventilators

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by Respironics.

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
    Safety alert
  • Date
    2012-08-02
  • Event Date Posted
    2012-08-02
  • Event Country
    Hong Kong
  • Event Source
    DH
  • Event Source URL
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20120802a.html
  • Notes / Alerts
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Extra notes in the data
    Medical Device Safety Alert
  • Reason
    Medical device safety alert: respironics trilogy 100, 200 and 202 ventilators the united states food and drug administration (fda) has issued a class i recall concerning respironics trilogy 100, 200 and 202 ventilators manufactured by respironics, inc. the affected model/ catalog numbers are 1032800, 1040004, 1040007, 1054096, 1054260, ca1032800, r1040004, r1054655, and 1045151. these specific units are being recalled because of the potential for a faulty component in the power supply. for details, please refer to fda website http://www.Accessdata.Fda.Gov/scripts/enforcement/ enforce_rpt-event-detail.Cfm?action=detail&id= 62393&w=08012012& if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 2 august 2012.

Device

Trilogy 100, 200 and 202 Ventilators
  • Model / Serial
  • Product Classification
    Anesthesiology Devices
  • Product Description
    Medical Device Safety Alert: Respironics Trilogy 100, 200 and 202 Ventilators
  • Manufacturer
    Respironics

Manufacturer

Respironics
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    DH