Siemens Healthineers Atellica IM 1600

Wash, Waste, or Fluidics System Fault Occurs

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Asset Type

Immunoassay Analyzer

Manufacturer

Siemens Healthineers

Model

Atellica IM 1600

What This Guide Helps With

Use this guide when wash, waste, liquid handling, or another fluidics condition prevents normal analyzer operation or produces repeated faults.

Step-by-Step Troubleshooting

1. Protect Patient Testing and Check for Leakage

Stop patient testing if the analyzer's fluidics cannot be trusted.

Immediately inspect for:

If significant leakage is present, stop troubleshooting and remove the analyzer from service.

Expected outcome: The analyzer is confirmed safe for limited external inspection. Any significant leak results in immediate escalation.

2. Identify the Fluidic Condition

Determine whether the reported problem involves:

Record the exact displayed condition.

Expected outcome: The affected fluid pathway or consumable category is identified.

3. Verify External Fluid Supplies

Inspect applicable externally accessible fluid containers or supplies.

Confirm:

Do not substitute unapproved fluid.

Expected outcome: Required external fluids are present and correctly connected. If restoring a missing or disconnected supply resolves the fault, troubleshooting can stop after verification.

4. Verify Waste Condition

Inspect the waste system components accessible to normal maintenance.

Check for:

Follow appropriate biological and chemical safety precautions.

Expected outcome: Waste can be safely collected and routed without visible obstruction. If correcting the external waste condition clears the fault, proceed to verification.

5. Inspect Accessible Tubing and Connections

Without removing internal panels, visually inspect accessible fluid lines and connectors for:

Do not disconnect internal fluid lines unless the procedure is explicitly authorized.

Expected outcome: Accessible tubing is intact and correctly routed. A simple external connection problem can be corrected and verified.

6. Check Consumables and Maintenance Status

Confirm any required wash-related consumables are installed and that no routine operator-level maintenance condition has been missed.

Review whether the problem occurred:

Expected outcome: External maintenance prerequisites are satisfied and the timing of the fault is understood.

7. Perform an Approved Prime or Recovery Function Only if Authorized

If normal operator or maintenance procedures provide an approved fluidics recovery, prime, or rinse function, perform it only after external causes have been corrected.

Do not repeatedly run recovery cycles against an unresolved leak, blockage, or empty supply.

Expected outcome: The fluidics system completes the approved recovery process without recurrence of the fault. If so, continue to final verification.

8. Verify Analyzer Operation

Using suitable nonpatient material, verify:

Expected outcome: Fluidics operation is stable and required laboratory checks are satisfactory. Troubleshooting can stop.

9. Escalate Persistent Fluidics Faults

If external supplies, waste, tubing, consumables, and approved recovery actions are normal but the fault returns, remove the analyzer from service.

Do not disassemble internal pumps, valves, tubing manifolds, or liquid sensors unless trained and authorized.

Expected outcome: A likely internal fluidics condition is documented and escalated.

If the Problem Persists

If fluid supplies, waste handling, accessible tubing, consumables, visible leaks, and approved external recovery steps have been verified, common external causes have been ruled out.

Remaining possibilities include internal pump, valve, pressure, flow, liquid-sensing, tubing, drainage, or control problems.

The analyzer should be:

After repair, inspect for leaks, verify fluid handling, complete appropriate functional testing, and confirm required QC before patient testing resumes.

Knowing when to stop external troubleshooting is proper troubleshooting.

Clinical Use Tip

Treat any significant analyzer fluid leak as both an equipment and contamination hazard; remove the system from use rather than continuing operation.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"Laboratory staff reported a recurring waste-system fault on the Atellica IM 1600 that stopped sample processing."

Cause

What was observed during troubleshooting.

Example:
"Clinical Engineering found the external waste container was full and not allowing normal waste handling."

Resolution

What action was taken.

Example:
"Waste was handled according to facility procedure, the container was correctly reinstalled, analyzer fluidics operated normally, and required verification was completed."

Helpful Details to Include (If Known)

Final Thought

Fluidics troubleshooting should begin with safety, leaks, supplies, waste, and visible tubing before considering internal pumps or valves. Stable fluid handling and successful verification are required before the analyzer returns to patient testing.

That is successful troubleshooting.

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