Recall Or Safety Alert for Transesophageal transducers (ETE) model MPT7-4 codes 4000-0317-01 to 4000-0317-19, manufactured by Philips Ultrasound Inc., USA, used with the ultrasound systems ATL UM9, ATL HDI 3000, ATL HDI 3500, ATL HDI 5000 and Philips 5000.

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 Philips Ultrasound 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
    Recall / Safety Alert
  • Date
    2015-01-23
  • Event Country
  • 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
    Recommendations for the verification and verification of transesophageal transducers (ETE) model MPT7-4, manufactured by Philips Ultrasound Inc., USA, in the case that they are temporarily used after the end of their service period.

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    AEMPSVFOI