Events

Recall of da Vinci Surgical Systems User Manuals Instruments and Accessories User Manual 550675, da Vinci Reprocessing User Manual 550875, da Vinci User Manual IS1200 550139, da Vinci User Manual IS2000 550516, da Vinci User Manual IS3000 550650

According to Valvira - National Supervisory Authority for Welfare and Health (via FOI), this recall involved a device in Finland that was produced by Intuitive Surgical.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    2012-0435
  • Date
    2012-05-15
  • Event Country
    Finland
  • Event Source
    VNSAWH
  • Notes / Alerts
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Extra notes in the data
    Source: NCAR
  • Reason
    Device failure / feature before use - instructions.

Device

da Vinci Surgical Systems User Manuals Instruments and Accessories User Manual 550675, da Vinci R...

Manufacturer

Intuitive Surgical