Events

Safety Alert for BIOSENSE WEBSTER Dirigible Guides

According to National Institute of Drugs and Food Surveillance (INVIMA), this safety alert involved a device in Colombia that was produced by Cordis Corporation || Codman & Shurtleff Inc. || Nitinol Devices And Components Inc || Greatbatch Medical || Argon Medical Devices, 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
    R1702-67
  • Event Number
    2009DM-0004835
  • Date
    2017-02-21
  • Event Country
    Colombia
  • Event Source
    INVIMA
  • Event Source URL
    https://app.invima.gov.co/alertas/dispositivos-medicos-invima?page=100
  • 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 states that it has detected that one side of the package may not be sealed, resulting in a compromise of the sterile barrier of the device, leading to possible adverse events on the patient.

Device

BIOSENSE WEBSTER Dirigible Guides

Manufacturer

Cordis Corporation || Codman & Shurtleff Inc. || Nitinol Devices And Components Inc || Greatbatch...
  • Source
    NIDFSINVIMA