COULTER GEN*S System, Part Number: 6605381, Beckman Coulter, Brea, CA. (Hematology analyzer)
FDA Recall Z-0315-2008 · Posted 2007-12-22
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Recalling FirmBeckman Coulter Inc
Recall StatusTerminated
Product CodeGKL
Date Initiated2007-04-18
Date Terminated2012-04-16
Product Quantity815 units to the US; 95 units to Canada
Reason for Recall
Patient Mis-identification can occur:
1)- When a positive identifier (Sample ID or Cassette/Position) is manually edited to a positive identifier that is already in the To Do list. The workstation will accept the entry and no error message will be generated, creating 2 samples with the identical positive identifier.
2)- When manually entering a Patient ID, if a blank space is entered between th
Firm Action
Product Corrective Action (PCA) letters were mailed
on April 18,2007, to all GENS, LH500, LH750 and
LH780 accounts. They are informed that a potential
misidentification can occur in 2 scenarios.
1. When a positive identifier (Sample ID or
CassetteIPosition) is manually edited to a
positive identifier that is already in the ToDo list.
The workstation will accept the entry and no
error message will be generated, creating 2
samples with the identical positive identifier.
2. When manually entering a Patient ID, if a blank
space is entered between the characters in the
Patient ID field, the system will only accept the
characters before the space.----Short term fix-----
The letter explains the issues and provides the
customer work around. (Letters were sent by US
mail). A customer response form was provided. The root cause of the problem is still under investigation, software upgrades, when approved will be made to devices.
Root Cause
Software design
Distribution Pattern
World wide: USA and Canada
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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