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
    30203
  • Event Risk Class
    III
  • Event Initiated Date
    2017-03-06
  • 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
    In isolated cases when ecrea is processed immediately after the weekly automated acid clean routine during probe test there is the remote potential for an elevation of greater than 15 percent in the ecrea result. investigation has determined that the processing of ecrea quality control (qc) after the probe test will identify a potential elevated ecrea result.

Device

  • Model / Serial
    Model Catalog: 1000033793 (Lot serial: > 10 contact mfg.); Model Catalog: 1000034648 (Lot serial: > 10 contact mfg.)
  • Product Description
    DIMENSION VISTA 1500 Intelligent Lab System;DIMENSION VISTA 500 INTELLIGENT LAB SYSTEM
  • Manufacturer

Manufacturer

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