Events

Recall Or Safety Alert for Disposable pediatric tubing VentStar Oxylog3000F (P) 190, reference 5704964

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 Drägerwerk AG & Co.KGaA.

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
    2016-06-14
  • 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
    Removal from the market of VentStar Oxylog3000F (P) 190 disposable pediatric tubing, reference 5704964, manufactured by Drägerwerk AG & Co.KGaA, Germany and used with the Oxylog 3000 and Oxylog 3000 Plus ventilators.

Device

Disposable pediatric tubing VentStar Oxylog3000F (P) 190, reference 5704964

Manufacturer

Drägerwerk AG & Co.KGaA