
Beckman Coulter · Model Allegra X-12 Series
Save time and labor. Eliminate 15 mL or 50 mL conical tubes. Reduce a potential contamination step Complete Your Run--Even with Imbalance. ARIESTM Smart Balance Rotor automatically corrects for imbalance. Up to 50 grams opposing loads. Eye balance your samples with confidence Save Time with a Truly Intuitive Interface. Avoid scrolling. User-friendly prompts.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Error code, run will not begin, or aborts shortly after start.
Root cause: Set speed exceeds the rotor maximum, an imbalanced load, the lid / door not locked, an unapproved rotor, or a drive / control fault.
Symptoms: Slow spin-up, rumble, or vibration during a run.
Root cause: Load imbalance, worn drive / motor bearings, a worn drive coupling, or (older units) worn motor brushes.
Symptoms: Run ends early / late, or RPM does not match the setting.
Root cause: Tacho / speed-sensor drift or a control-board fault.
Symptoms: Lid-lock error, will not open after a run, or will not lock to start.
Root cause: Lid-lock solenoid / switch fault, or a run still winding down.
Symptoms: Visible corrosion, cracks, or a bucket that will not swing; imbalance trips.
Root cause: Rotor / bucket ageing - a safety-critical wear item with a use-life limit.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
Log rotor runs; retire per the manufacturer's rotor-life programme.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Drive / motor bearings & coupling | Major service part | $$$ | Difficult |
| Lid-lock solenoid / switch | Major service part | $$ | Moderate |
| Speed sensor / control board | Major service part | $$ | Moderate |
| Motor brushes (older units) | Periodic replacement | $ | Moderate |
| Rotor / bucket set & O-rings Log rotor runs; retire per the manufacturer's rotor-life programme. | Major service part | $$$ | Easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
Extracted directly from this unit's own service manual.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
Synced live from the FDA openFDA API.
Beckman Coulter has become aware of an intermittent issue in which the optional flag Previous Sample Had Sperm was enabled but not displayed so that a carryover event could have been investigated.
Beckman Coulter has determined that there is a potential for under-reporting casts. This can occur if per high-power field (/HPF) units of measurement for casts are selected in the iQ200 software, but the abnormal threshold and/or grading format is set up based on reporting per low-power field (/LPF)* or *per microliter. This may occur during initial method validation or if settings are altered after the initial validation.
Unpaired lots of AU lyophilized chemistry calibrator level 1 and 2 have been distributed. Calibrator level 1 and 2 must be paired when used for calibration and cannot be used in any other combination. If lot numbers are not correctly paired, calibration can be run using incorrect set points which may generate erroneous results. QC failures could occur if incorrect pairs of calibrators are used.
The recall was initiated after Beckman Coulter identified four (4) issues with the COULTER LH 500 Series System and the Unicel DxH 800 Coulter Cellular Analysis System: Issue 1: There is a potential for misidentification to occur when the system is configured in languages other than English or Chinese. The characters #,@,[,\,],`,{,|,}, or ~ are substituted or omitted in other languages. The issu
Beckman Coulter has become aware of a potential issue in which the Sample ID information embedded in the barcode affixed to a slide made by the Coulter GEN*S and LH SlideMaker does not match the text.
There is a potential for erroneous yet credible results for Body Fluids on the LH700 series hematology analyzers when a cassette label fails to read and the subsequent sample is cycled in Body Fluid mode.
There is a risk of sample misidentification when processing samples in the Manual aspiration mode.
Biohazard situation exists for users.
Incorrect Hemoglobin result can be reported with software version 2A and higher.
Software vote out logic changed. Erroneous white blood cell counts.
From BioLab, for work done with this kind of equipment.
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