
GEGeneric · Model FACSCount
Easy to Install, Set Up, and Run with Confidence The BD FACSCount system is easy to install. The instrument operates from a standard electrical outlet, requiring no hardware adjustments or calibration. Only minimal training is needed to set up the instrument and to run samples. Simple prompts on the display guide operators through testing, from input of patient information to final results. The software automatically identifies the lymphocyte populations of interest and summarizes patients’ results in a printed sample report. Quality controls in the software ensure that reported results are accurate by detecting and flagging error conditions and suppressing results when control limits are exceeded. Results are objective, requiring no interpretation or subjective analysis by the operators. Quality control To validate laboratory practice and methodology, BD FACSCount™ control beads can be added to samples prepared with normal blood. BD FACSCount fluorescent reference beads are included in the reagent tube, and ensure accurate enumeration of lymphocytes of interest with no operator intervention. The control run generates a detailed analysis in a printed report summarizing system performance. The result of the last control run is reported on subsequent sample printouts to help determine linearity and pipetting accuracy. Since absolute counts are calculated from directly measured cell counts and reference bead counts on the BD FACSCount system, no additional analysis on a hematology analyzer is necessary. Simplified sample handling Sample preparation follows an easy three-step process. First, blood is added to a tube that contains pre-measured reagents. Then the sample is vortexed and incubated. In the second step, a fixative is added to the tube, and then it is vortexed and incubated. In step three, the sample is vortexed and run on the instrument. Easy three-step sample preparation Prepare controls and patient samples by adding blood, then fixative solution, to the reagent tubes.
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: Bead CVs out of spec, scatter or fluorescence signal low or noisy, compensation drift.
Root cause: Flow-cell contamination or an air bubble, laser degradation / misalignment, or an optics / PMT fault.
Symptoms: Unstable event rate, boost / prime failures, sheath or waste alarm, clogs.
Root cause: Sheath / waste tank issue, a peristaltic / vacuum fault, or a partially blocked sample line / flow cell.
Symptoms: No or low event rate, probe-position error, carryover.
Root cause: Clogged or bent sample probe, or a clot.
Symptoms: A laser-line-specific parameter fails, laser-error message.
Root cause: Laser at end of life or a power-supply / interlock fault.
Symptoms: Acquisition hangs, data will not export, instrument not recognised.
Root cause: Workstation PC or the acquisition software / link.
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.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Flow cell | Periodic replacement | $$$ | Difficult |
| Sample probe / SIP | Periodic replacement | $$ | Moderate |
| Peristaltic pump tubing | Frequent wear item | $ | Moderate |
| Sheath / waste filters | Frequent wear item | $ | Easy |
| Laser | Periodic replacement | $$$$ | Difficult |
Relative cost: $ lowest · $$$$ 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.
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.
From BioLab, for work done with this kind of equipment.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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