Events

Recall Or Safety Alert for Applicators and accessories of high dose rate deferred load equipment (HDR): Set esophageal applicator (Set 0119), Bougie applicator, esophagus 8mm (LAZ24-08), Bougie applicator for esophagus 10mm (LAZ24-10) and applicator Bougie for esophagus 12mm (LAZ24-

According to Agencia Española de Medicamentos y Productos Sanitarios (Via FOI), this recall or safety alert involved a device in Spain that was produced by Eckert & Ziegler BEBIG GmbH.

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
    Recall / Safety Alert
  • Date
    2016-05-19
  • Event Country
    Spain
  • Event Source
    AEMPSVFOI
  • Notes / Alerts
    The data from Spain is current through June 2018. All of the data comes from Agencia Española de Medicamentos y Productos Sanitarios, 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 Spain.
  • Extra notes in the data
  • Action
    Possible deviation in the dose of radiation administered with the high dose rate deferred load (HDR) equipment, manufactured by Eckert & Ziegler BEBIG GmbH, Germany, because the central channel of certain Bougie esophage applicators is not uniformly centered.

Device

Applicators and accessories of high dose rate deferred load equipment (HDR): Set esophageal appli...

Manufacturer

Eckert & Ziegler BEBIG GmbH