Safety Alert for Transport ventilator

According to National Institute of Drugs and Food Surveillance (INVIMA), this safety alert involved a device in Colombia that was produced by Weinmann Emergency Medical Technology Gmbh + Co-Kg.

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
    I1605-217
  • Event Number
    2014EBC-0012502
  • Date
    2017-05-25
  • Event Country
  • Event Source
    INVIMA
  • 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 reports that it has detected several cases of degustation in the gray accessories belonging to the patient circuits of 2 meters, previously referred to, which could lead to the potential occurrence of adverse events on patients due to ventilatory insufficiency.

Device

  • Model / Serial
    Concerning circuits to patient references WM 28285, WM 28435, WM 28695, WM 28690, WM 28657, WM || 28483, WM 28865, WM 29195, WM 28907 and WM 29192.
  • Product Description
    MEDUMAT is a device to mechanically assist spontaneous pulmonary ventilation when it is non-existent, ineffective for life
  • Manufacturer