Events

Recall Or Safety Alert for ProAQT cardiac output sensor

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 Pulsion Medical Systems SE.

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
    2015-03-20
  • 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
    Extension of the market recall to batch 14IC05 of the cardiac output sensor ProAQT, reference PV8810, manufactured by Pulsion Medical Systems SE, Germany, due to its possible contamination by damages in the primary packaging of the device.

Device

ProAQT cardiac output sensor

Manufacturer

Pulsion Medical Systems SE
  • Manufacturer Parent Company (2017)
    Getinge AB
  • Source
    AEMPSVFOI