Events

Recall Or Safety Alert for "Astrada intrathecal catheter with 86 cm intraspinal segment" (model 8780), "Ascenda intrathecal catheter with 66 cm intraspinal segment" (model 8781) and "Ascenda revision kit" (model 8784)

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 N/A.

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
    2014-07-24
  • Event Country
    Spain
  • Event Source
    AEMPSVFOI
  • Event Source URL
    N/A
  • 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 certain serial numbers of the products "Astrada intrathecal catheters" (models 8780 and 8781) and "Ascenda revision kit" (model 8784), due to the possibility of failure of the catheter retention ring

Device

"Astrada intrathecal catheter with 86 cm intraspinal segment" (model 8780), "Ascenda intrathecal ...
  • Model / Serial
  • Manufacturer
    N/A

Manufacturer

N/A
  • Source
    AEMPSVFOI