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Terminated

CXP software for Cytomics FC500 Cytometer

FDA Recall Z-0266-05 · Posted 2004-11-30

Recalling FirmBeckman Coulter Inc
Recall StatusTerminated
Product CodeGKZ
Date Initiated2004-11-02
Date Terminated2012-05-08
Product Quantity167

Reason for Recall

Incorrect sample identification can be displayed and printed on the Runtime Panel Report due to a software defect.

Firm Action

The Product Corrective Action Customer Letter which includes Modified Operating Instructions was sent to US and Canadian customers the week of November 8, 2004 via US Mail.

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.

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