Safety Alert for Patient Monitor MINDRAY

According to National Institute of Drugs and Food Surveillance (INVIMA), this safety alert involved a device in Colombia that was produced by Shenzhen Mindray Bio-Medical Electronics 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
    Safety alert
  • Event ID
    I1704-141
  • Event Number
    2009EBC-0003486
  • Date
    2017-04-25
  • 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 has reported a possible problem of overheating of the rechargeable lithium-ion battery used in the referenced equipment, the failure mode can result in overheating of the battery by throwing sound and visual alarm of "without battery", leading to possible occurrences adverse events about patients.

Device

  • Model / Serial
  • Product Description
    Indicated for monitoring vital parameters of adult, pediatric and neonatal patients during their stay in clinic. Intensive care, intermediate care unit, surgery rooms, observation units and post operative are used.
  • Manufacturer

Manufacturer