Recall of ADVIA CHEMISTRY SYSTEM - ACETAMINOPHEN (ACET) ASSAY

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
    82316
  • Event Risk Class
    III
  • Event Initiated Date
    2015-06-30
  • 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
    Change in the concentration of n-acetylcysteine (nac) that may cause interference for the advia chemistry systems acetaminophen assay for the lots listed. this issue applies to the advia 1200 1800 and 2400 chemistry systems and advia chemistry xpt systems.

Device

  • Model / Serial
    Model Catalog: 07989138 (Lot serial: 47001); Model Catalog: 07989138 (Lot serial: 46782); Model Catalog: 07989138 (Lot serial: 46370); Model Catalog: 07989138 (Lot serial: 46369); Model Catalog: 07989138 (Lot serial: 46564); Model Catalog: 07989138 (Lot serial: 46619); Model Catalog: 07989138 (Lot serial: 46251)
  • Product Description
    ADVIA CHEMISTRY SYSTEM
  • Manufacturer

Manufacturer

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