Safety Alert for Lifepak

According to National Institute of Drugs and Food Surveillance (INVIMA), this safety alert involved a device in Colombia that was produced by Physio Control, Inc.

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
    A1608-352
  • Event Number
    2012EBC-0008670
  • Date
    2016-08-19
  • 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 informs that it has detected that the referenced equipment may fail to initiate voice messages, press the on / off button and when the rear cover is opened the switch is closed, condition in which the equipment will not discharge, which may lead to the occurrence of potentially serious adverse events on the patient.

Device

  • Model / Serial
    LIFEPAK EXPRESS AED and LIFEPAK CR PLUS AED
  • Product Description
    It provides stimulation to the heart for the automatic treatment of ventricular arrhythmias that endanger the life of the patient and when they exhibit symptoms of sudden parocardia.
  • Manufacturer

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    NIDFSINVIMA