Events

Recall of DIMENSION VISTA SYSTEM - DIMENSION VISTA 1500 ANALYZER

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
    19933
  • Event Risk Class
    III
  • Event Initiated Date
    2011-12-21
  • 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
    Dimension vista software version 3.4 for below manufacturer assay range erroneously flags patient test results that that are within the assay range as defined in the instructions for use for the respective method. this issue is isolated to vista software version 3.4. customers who have not made any changes to the default method configurations.

Device

DIMENSION VISTA SYSTEM - DIMENSION VISTA 1500 ANALYZER
  • Model / Serial
    Model Catalog: 1000035896 (Lot serial: SOFTWARE VERSION 3.4); Model Catalog: 1000036563 (Lot serial: SOFTWARE VERSION 3.4)
  • Product Description
    DIMENSION VISTA 1500 ANALYZER
  • Manufacturer
    SIEMENS HEALTHCARE LIMITED

Manufacturer

SIEMENS HEALTHCARE LIMITED
  • Manufacturer Address
    OAKVILLE
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    HC