Events

Safety Alert for System for High Permeability Hemodialysis PRISMAFLEX

According to National Institute of Drugs and Food Surveillance (INVIMA), this safety alert involved a device in Colombia that was produced by Gambro Lundia 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
    I1806-377
  • Event Number
    2010EBC-0006651
  • Date
    2018-06-07
  • Event Country
    Colombia
  • Event Source
    INVIMA
  • Event Source URL
    https://app.invima.gov.co/alertas/dispositivos-medicos-invima?page=43
  • 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

Device

System for High Permeability Hemodialysis PRISMAFLEX
  • Model / Serial
    PRISMAFLEX SYSTEM, PRISMAFLEX 7.XX Row, PRISMAFLEX 6.10
  • Product Description
    The PRISMAFLEX control unit is indicated for: Continuous Renal Replacement Therapy (CRRT) for Patients Therapeutic Exchange of Plasma (TPE) for patients with disorders in which the withdrawal of the components of the plasma.
  • Manufacturer
    Gambro Lundia Ab

Manufacturer

Gambro Lundia Ab