Recall of DIMENSION VISTA SYSTEM - V-LYTE INTEGRATED MULTISENSOR - NA K CL

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
    54493
  • Event Risk Class
    III
  • Event Initiated Date
    2017-04-24
  • 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 has confirmed an increase in complaints regarding elevated urine sodium quality control (qc) exceeding acceptable qc ranges with the dimension vista imt system. siemens observed a greater urine sodium drift with urine qc than urine patient samples. not all imt sensors exhibit the described urine sodium qc drift. current lots and all future lots are potentially affected until this issue is resolved.

Device

  • Model / Serial
    Model Catalog: K800A (Lot serial: >10 CONTACT MANUFACTURER)
  • Product Description
    V-LYTE Integrated Multisensor Technology (IMT)
  • Manufacturer

Manufacturer

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