Events

Recall of THE BELMONT RAPID INFUSER SYSTEM FMS2000 - FLUID MANAGEMENT SYSTEM

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BELMONT INSTRUMENT CORPORATION.

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
    90927
  • Event Risk Class
    II
  • Event Initiated Date
    2012-10-01
  • 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
    There is a potential that fluid spills may result in an accumulation of salt build up on the power entry area and may result in the remote potential of an electrical flash occurring.

Device

THE BELMONT RAPID INFUSER SYSTEM FMS2000 - FLUID MANAGEMENT SYSTEM
  • Model / Serial
    Model Catalog: 903-00023 (120V) (Lot serial: >10 numbers contact mfg); Model Catalog: 903-00001 (Lot serial: >10 numbers contact mfg); Model Catalog: 903-00001A (230V) (Lot serial: >10 numbers contact mfg)
  • Product Description
    The Belmont Rapid Infuser FMS2000
  • Manufacturer
    BELMONT INSTRUMENT CORPORATION

Manufacturer

BELMONT INSTRUMENT CORPORATION