Recall of ADVIA CENTAUR XP SYSTEM - INSTRUMENT CLASS 2

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

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
    111333
  • Event Risk Class
    III
  • Event Initiated Date
    2014-08-20
  • Event Country
  • 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
    Manufacturer advises that a specific scenario has been identified that causes patient demographics data (patient name age sex) from the previous order received from the laboratory information system(lis) to be merged with the next order. the incorrect patient demographics data will display on the advia centaur/advia centaur xp user interface print on instrument-generated reports and will be transmitted to the lis with the test result.

Device

  • Model / Serial
    Model Catalog: 09066916 (Lot serial: ALL); Model Catalog: 078-A010-07 (Lot serial: ALL); Model Catalog: 04911855 (Lot serial: ALL); Model Catalog: 078-A001-14 (Lot serial: ALL)
  • Product Description
    ADVIA CENTAUR XP SYSTEM - INSTRUMENT CLASS 2
  • Manufacturer

Manufacturer

  • Manufacturer Address
    OAKVILLE
  • Manufacturer Parent Company (2017)
  • Source
    HC