Events

Recall of UROSKOP ACCESS SYSTEM

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SIEMENS CANADA LIMITED - HEALTHCARE.

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
    55065
  • Event Risk Class
    III
  • Event Initiated Date
    2004-06-18
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Extra notes in the data
  • Reason
    Imaging system software update va14a/.

Device

UROSKOP ACCESS SYSTEM
  • Model / Serial
    Model Catalog: 57 56 130 J1052 (Lot serial: 1051); Model Catalog: 57 56 122 J1052 (Lot serial: 1051); Model Catalog: 57 56 122 J1052 (Lot serial: SN 2019); Model Catalog: 57 56 122 J1052 (Lot serial: 2033); Model Catalog: 57 56 130 J1052 (Lot serial: SN 2019); Model Catalog: 57 56 130 J1052 (Lot serial: 2033)
  • Product Description
    UROSKOP ACCESS - X-RAY SYSTEM
  • Manufacturer
    SIEMENS CANADA LIMITED - HEALTHCARE

Manufacturer

SIEMENS CANADA LIMITED - HEALTHCARE
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    HC