Events

Recall of IVAC SE II VOLUMETRIC INFUSION PUMP - 7200/7230

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by MAQUET-DYNAMED 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
    38953
  • Event Risk Class
    II
  • Event Initiated Date
    2004-03-22
  • 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
    Prior to nov 1998 safety alert it had been determined that there had been a total of 8 complaints related to improper installation of mechanism spring. complaint date ranged from dec 96 to aug 98. no can comp.

Device

IVAC SE II VOLUMETRIC INFUSION PUMP - 7200/7230
  • Model / Serial
    Model Catalog: 7230 (Lot serial: 3571481)
  • Product Description
    ivac SE II volum.infusion pump
  • Manufacturer
    MAQUET-DYNAMED INC.

Manufacturer

MAQUET-DYNAMED INC.
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Getinge AB
  • Source
    HC