Safety Alert for anesthesia system Flow-I

According to National Institute of Drugs and Food Surveillance (INVIMA), this safety alert involved a device in Colombia that was produced by Maquet Critical Care Ab.

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
  • Event ID
  • Event Number
  • Date
  • Event Country
  • Event Source
  • Event Source URL
  • Notes / Alerts
    Colombian data is current through June 2019. All of the data comes from the National Institute of Drugs and Food Surveillance (INVIMA), 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 Colombia.
  • Extra notes in the data
  • Reason
    The manufacturer that there is a risk of leakage due to the accidental displacement of the cassette of the patient, leading to the occurrence of potentially adverse events on the patients.


  • Model / Serial
    FLOW-i, serials before 2753
  • Product Classification
  • Product Description
    Intended for the administration of anesthesia while controlling the complete ventilation of patients with no ability to breathe, as well as in the support of patients with limited ability to breathe.
  • Manufacturer


  • Manufacturer Parent Company (2017)
  • Source