Beckman Coulter ACL 8000
Beckman Coulter · Model ACL 8000
Extensive test menu and advanced robotics for heightened precision and accuracy. The ACL 8000 coagulation analyzer features an extensive test menu and advanced robotics for heightened precision and accuracy. For monitoring hemostatic disorders, approximately 40 clotting, immunoturbidimetric and chromogenic assays are available on the system, including tests for D-Dimer, Von Willebrand Antigen and Free Protein S. The system can perform a D-Dimer test in less than 10 minutes. Laboratorians also can combine test selections to obtain PT, APTT and fibrinogen results on up to eight samples in less than 10 minutes. To improve accuracy of results, the ACL 8000 offers automated reflex and rerun testing capabilities, while the system's clot signature curve technology aids in clinical interpretation of test results and troubleshooting.
Key tips
- ·Run QC controls before trusting any repair - an analyzer that passes self-test can still report clinically wrong results.
- ·Rule out a reagent lot change before opening the instrument - it can look exactly like a hardware fault.
- ·Centrifuge rotors have a hard retirement age/cycle limit regardless of visible condition - don't eyeball it.
Typical Failure Modes
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.
Aperture / flow-cell blockage or partial obstruction
HighSymptoms: Flagged or implausible CBC counts, voteouts, clog alarms, poor precision.
Root cause: Debris or a clot partially blocking a counting aperture or the flow cell.
Sample probe / piercer / valve wear
MediumSymptoms: Short samples, aspiration errors, cap-piercing failures, carryover.
Root cause: Worn or bent sample probe / closed-vial piercer, or a worn shear / segment valve.
Reagent / lyse delivery fault
MediumSymptoms: WBC, HGB or diff results shifted, high background, reagent alarms.
Root cause: Reagent depleted or wrong lot, or a pinch-valve / tubing fault.
Optics / laser fault (diff)
MediumSymptoms: Diff scattergrams abnormal, missing populations, flow-cell or laser alarm.
Root cause: Contaminated or aged flow cell, or the laser / optics.
Vacuum / pressure out of range
MediumSymptoms: Multiple parameter errors, priming failures.
Root cause: Pump or regulator drift.
Serviceable Parts & Consumables
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.
Sample probe / closed-vial piercer
Class Periodic replacementRel. cost $$R&R Moderate
Shear / segment valve
Class Periodic replacementRel. cost $$$R&R Difficult
Pinch-valve / peristaltic tubing
Class Frequent wear itemRel. cost $R&R Moderate
Flow cell
Class Periodic replacementRel. cost $$$R&R Difficult
System reagents / controls
Class ConsumableRel. cost $$R&R Easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Sample probe / closed-vial piercer | Periodic replacement | $$ | Moderate |
| Shear / segment valve | Periodic replacement | $$$ | Difficult |
| Pinch-valve / peristaltic tubing | Frequent wear item | $ | Moderate |
| Flow cell | Periodic replacement | $$$ | Difficult |
| System reagents / controls | Consumable | $$ | Easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
PM Checklist
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.
- ·Daily QC controls run and reviewed
- ·Calibration verification per assay
- ·Routine cleaning and decontamination
- ·Scheduled reagent-path and pump-tubing maintenance
Troubleshooting Approach
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.
Symptom: Clog alarm or flagged counts
- Run the instrument's aperture / flow-cell clear and flush cycles.
- Run a background count and confirm it is within limits.
- Run controls at all levels.
- Clean or replace the aperture bath / flow cell if clogs recur.
- Confirm precision on a replicate sample before releasing results.
Symptom: Short samples or aspiration errors
- Inspect the sample probe / piercer for wear or a bend.
- Check the shear / segment valve and tubing for leaks or wear.
- Verify vacuum and pressure against the service spec.
- Replace the probe / piercer, valve or tubing as found.
- Re-run controls.
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Central / core laboratory
- Point-of-care testing stations
- Blood bank
- Microbiology lab
Documents & Manuals
No documents available for this device yet.
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
The recall was initiated because Beckman Coulter has confirmed that the stated stability of the DSL-10-8000 I-PTH ELISA and DSL-8000 I-PTH IRMA assays may not be achieved for the lot numbers affected by the recall. The affected I-PTH ELISA and the I-PTH IRMA kit lots may produce falsely elevated patient results. Internal stability testing showed an average 16% elevation for I-PTH ELISA lot 99
- RECALL
The recall was initiated after Beckman Coulter confirmed that the stated stability of the DSL-10-8000 I-PTH ELISA assay may not be achieved for lot numbers: 891198, 990980 and 991448. The kit lot numbers listed above passed the stability testing performed at 6 months, but failed the testing performed at 12 months. Therefore the affected I-PTH ELISA kit lots may produce falsely elevated patient r
Troubleshoot this device with Bio
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
Ask Bio