Recall of CS300 INTRA AORTIC BALLOON PUMP SYSTEM - MAIN UNIT

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
    18965
  • Event Risk Class
    III
  • Event Initiated Date
    2010-05-12
  • 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
    Maquet/datascope has identified an uncharacteristic increase in the number of screen display related issues reported on the intra-aortic balloon pumps (iabp). the display controller assembly with date code 08_05 was defective and is associated with this issue. we are recalling iabp's manufactured with the display controller assembly date code 08_05. this issue may cause the iabp to exhibit display distortion 'pixeling' and blanking. although the iabp continues to deliver therapy to the patient these issues cause the user to be unable to read the information that is being displayed.

Device

  • Model / Serial
    Model Catalog: 0998-00-3023-XX (Lot serial: SI135828G8)
  • Product Description
    CS300 INTRA-AORTIC BALLOON PUMP
  • Manufacturer

Manufacturer

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