Z-0259-05

CXP Software Version 1.0 and 1.1 (operating software for Cytomics FD500 Cytometer. Part numbers: 624281...

Name: Z-0259-05 CXP Software Version 1.0 and 1.1 (operating software for Cytomics FD500 Cytometer. Part numbers: 624281...
Creator: Beckman Coulter Inc
Published: 2004-08-02
License: https://open.fda.gov/license/

Siemens Healthcare Diagnostics Inc. / initiated 2004-08-02 / Terminated / root cause: software

FDA source

Beckman Coulter Inc began a recall of CXP Software Version 1.0 and 1.1 (operating software for Cytomics FD500 Cytometer. Part numbers: 624281, 623560, 623563, 623554, 623555, 623541, 623556... on 2004-08-02. The reason FDA records is "Software anomaly". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as software.

Recall record

Recall number: Z-0259-05
Status: Terminated
Initiated: 2004-08-02
Posted: 2004-11-30
Terminated: 2012-05-08
Recalling firm: Siemens Healthcare Diagnostics Inc.
Product: CXP Software Version 1.0 and 1.1 (operating software for Cytomics FD500 Cytometer. Part numbers: 624281, 623560, 623563, 623554, 623555, 623541, 623556, 623557, 623558, 623559.
Product code: GKZ Counter, Differential Cell
Reason for recall: Software anomaly.
Root cause tag: software
FDA root cause: Other
Action: A recall letter and workaround solution were mailed August 2, 2004. Firm will initiate a software upgrade as well.
Quantity in commerce: 89
Distribution: Nationwide and Canada
Product codes and lots: Versions 1.0 and 1.1 Serial and lot numbers are not applicable.

Product code GKZ

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)