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 DIAGNOSTICS INC..

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
    20272
  • Event Risk Class
    III
  • Event Initiated Date
    2015-11-13
  • 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
    Siemens healthcare diagnostics is conducting a field corrective action for the advia centaur and advia centaur xp immunoassay systems glass rod sensor (smn 10327638) in the waste reservoir. a potential vacuum leak may occur around the glass rod sensor in the waste reservoir caused by the gasket on the housing of the glass rod sensor sliding out of position.

Device

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

Manufacturer

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