Events

Recall of V SERIES PATIENT MONITORING SYSTEM - DOCKING STATION

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by MINDRAY DS USA 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
    27977
  • Event Risk Class
    II
  • Event Initiated Date
    2014-01-27
  • 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 v dock power pins connecting the v series monitor to the v dock may lose spring tension potentially causing the screen to temporarily go blank lose communication with the central station (when one is in use) or shut down.

Device

V SERIES PATIENT MONITORING SYSTEM - DOCKING STATION
  • Model / Serial
    Model Catalog: 0998-00-1801-01 (Lot serial: EGL19008961); Model Catalog: 0998-00-1801-01 (Lot serial: EGL19008944)
  • Product Description
    V Series Monitoring System
  • Manufacturer
    MINDRAY DS USA INC.

Manufacturer

MINDRAY DS USA INC.