Events

Recall of SENTEC DIGITAL MONITOR SYSTEM - V-SIGN SENSOR 2

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by MCARTHUR MEDICAL SALES 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
    63731
  • Event Risk Class
    III
  • Event Initiated Date
    2015-04-20
  • 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
    The pco2 performance does not comply with sentec's quality standards for customer satisfaction. therefore this recall is for the return and replacement of impacted device(s). sentec's risk evaluation concludes no adverse safety impact for patient or user.

Device

SENTEC DIGITAL MONITOR SYSTEM - V-SIGN SENSOR 2
  • Model / Serial
    Model Catalog: VS-A/P/N (Lot serial: S/N: 315.284); Model Catalog: VS-A/P/N (Lot serial: S/N: 315.124)
  • Product Description
    Sentec Digital Monitor System - V-Sign Sensor 2
  • Manufacturer
    MCARTHUR MEDICAL SALES INC.

Manufacturer

MCARTHUR MEDICAL SALES INC.