Recall Or Safety Alert for CPXTM4 mammary tissue expander, medium profile 650 cc, without suture tabs, product code PN 354-8225, lot no. 6947019

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 Mentor.

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
    2016-09-12
  • 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
    Withdrawal from the market of batch 6947019 of the CPXTM4 breast tissue expander, medium profile 650 cc, without suture tabs, product code PN 354-8225, manufactured by Mentor, USA, because some units of that batch may contain an incorrect expander .

Manufacturer

  • Source
    AEMPSVFOI