Events

Safety Alert for Cobas KRAS Mutation Kit (CE-IVD)

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

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
    R-RD-01-01-15
  • Event Number
    2012RD-0002140
  • Date
    2015-01-02
  • Event Country
    Colombia
  • Event Source
    INVIMA
  • Event Source URL
    https://app.invima.gov.co/alertas/dispositivos-medicos-invima?page=190
  • 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
    Performance flaws of the cobas kras mutation kit reagent (ce-ivd).

Device

Cobas KRAS Mutation Kit (CE-IVD)
  • Model / Serial
  • Product Description
    Determination of related analytes in samples from the human organism
  • Manufacturer
    ROCHE

Manufacturer

ROCHE