Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

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.

FDA Recall Z-0259-05 · Posted 2004-11-30

Recalling FirmBeckman Coulter Inc
Recall StatusTerminated
Product CodeGKZ
Date Initiated2004-08-02
Date Terminated2012-05-08
Product Quantity89

Reason for Recall

Software anomaly.

Firm Action

A recall letter and workaround solution were mailed August 2, 2004. Firm will initiate a software upgrade as well.

Root Cause

Other

Distribution Pattern

Nationwide and Canada

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑