Recall of Cytomics MXP Software, Version 1.0, Part No. 623688.

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Beckman Coulter 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
  • Event ID
  • Event Risk Class
    Class 2
  • Event Number
  • Event Initiated Date
  • Event Date Posted
  • Event Status
  • Event Country
  • Event Terminated Date
  • Event Source
  • Event Source URL
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Counter, Cell, Automated (Particle Counter) - Product Code GKL
  • Reason
    Software anomaly. sample id and the run date may become fixed within a header on the flowpage printout. all samples subsequently run, with results printed using the flowpage print format, will have the fixed sample id and run date, rather than the correct sample id and run date.
  • Action
    Firm sent modified operating instructions to users on 13 February 2004.



  • Manufacturer Address
    Beckman Coulter Inc, 200 S Kraemer Blvd, Brea CA 92821-6208
  • Source