
Beckman Coulter · Model HMX A/L
VCS technology for automated differential and semi-automated reticulocyte counts delivers consistently reliable results Advanced software features for automated test review and management Simple, fast and sensitive screening for morphologic white cell abnormalities High correlation of data between all VCS systems in your core and satellite labs Rapid result turnaround time with 75 samples-per-hour throughput Easy-to-use software with one-touch start up and shut down Continuous auto-loading for complete walkaway operation Error-free patient ID barcode reading at the point of aspiration for fail-safe sample management Closed vial sampling of various tube sizes improves operator safety.
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: Flagged or implausible CBC counts, voteouts, repeated aperture-clog alarms.
Root cause: Debris or a clot partially blocking a counting aperture.
Symptoms: Short samples, aspiration errors, bent piercer, cap-piercing failures.
Root cause: Worn or bent sample probe / closed-vial piercer.
Symptoms: WBC or diff results shifted, high background, reagent-empty or pressure alarms.
Root cause: Reagent depleted or wrong lot, or a pinch-valve / tubing fault; note the LYSE III reagent-lot recall history.
Symptoms: Tubes not advancing, carousel or transport error.
Root cause: Worn autoloader belt or a mis-loaded rack.
Symptoms: Multiple parameter errors, priming failures.
Root cause: Pump or regulator drift.
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 |
|---|---|---|---|
| Sample probe / closed-vial piercer | Periodic replacement | $$ | Moderate |
| Peristaltic / pinch-valve pump tubing | Frequent wear item | $ | Moderate |
| Aperture bath assembly | Major service part | $$$ | Difficult |
| Autoloader belt | Periodic replacement | $$ | Moderate |
| System reagents / controls | Consumable | $$ | 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.
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.
The recall was initiated by Beckman Coulter because the COULTER LYSE III diff Lytic Reagent Lot number 101554F was released for distribution to customers between November 17 and December 1, 2010 prior to completion of QC testing.
The recall was initiated because Beckman Coulter has confirmed the Coulter MAXM, MAXM AL, HmX and HmX AL Analyzers omit the tilde (~) character when the tilde is used as part of the Sample 10 within a barcode label scanned by the primary mode barcode reader. There is a potential for Specimen or Patient misidentification to occur.
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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