STERIS V-PRO Series

POWER LOSS, UNEXPECTED SHUTDOWN, OR RESTART DURING CYCLE

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Asset Type

Sterilizer

Manufacturer

STERIS

Model

V-PRO Series

What This Guide Helps With

Troubleshooting shutdowns or restarts caused by facility power, connections, disconnects, circuit events, external devices, overheating, or internal electrical faults.

Step-by-Step Troubleshooting

1. Protect Staff, Patients, and the Interrupted Load

An interrupted cycle cannot be accepted as sterile.

Notify Sterile Processing leadership immediately.

Segregate the entire load for reprocessing.

Do not force the door or remove power again.

Allow automatic recovery and aeration to complete.

Redirect urgent loads to another verified sterilizer.

If smoke, burning odor, unusual heat, arcing, or liquid leakage is present, disconnect power only when safe and follow emergency procedures.

Expected outcome: Personnel are protected and no instrument from the interrupted cycle enters patient care.

2. Confirm the Exact Power Event

Determine whether the sterilizer:

Lost all power.

Restarted automatically.

Displayed a low-power or recovery message.

Shut down only during a specific phase.

Affected room lights or other equipment.

Tripped a breaker or facility disconnect.

Produced an alarm, sound, odor, or visible sign before shutdown.

Record the cycle phase and approximate time of interruption.

Expected outcome: The event is classified as facility-wide, circuit-specific, connection-related, or isolated to the sterilizer.

3. Allow Safe Cycle Recovery

If the sterilizer has power:

Do not initiate another cycle.

Allow the unit to complete any automatic recovery.

Observe door lock status and displayed instructions.

Preserve the aborted-cycle record.

Open the chamber only when the sterilizer indicates it is safe.

Expected outcome: The chamber reaches a safe state and the interrupted load remains clearly identified as failed.

4. Check for a Facility-Wide Power Issue

Ask whether:

Lights flickered.

Other equipment restarted.

Emergency power transferred.

Maintenance was performed.

A generator test or utility disturbance occurred.

The area experienced a brief outage.

Coordinate with Facilities to review the event.

Expected outcome: A facility power event is confirmed or ruled out. If power is stabilized, continue with required verification before returning the sterilizer to use.

5. Inspect the External Power Connection

When the sterilizer is idle and safe:

Verify the plug or hardwired disconnect is fully engaged and undamaged.

Inspect accessible cords, plugs, strain relief, and receptacles.

Check for looseness, discoloration, heat damage, or arcing marks.

Confirm the disconnect was not accidentally operated.

Do not use adapters, extension cords, or temporary power strips.

Expected outcome: The external supply connection is secure and free of visible damage. Damaged power components require immediate removal from service.

6. Check the Branch Circuit and Breaker Status

Coordinate with Facilities or qualified electrical personnel.

Determine whether the circuit breaker tripped.

Identify other equipment on the same circuit.

Do not repeatedly reset a breaker that trips.

Confirm the sterilizer is connected to the approved dedicated electrical source when required by the installation.

Document voltage-quality testing only when performed by qualified personnel using approved equipment.

Expected outcome: The circuit remains stable and appropriately supports the sterilizer. Repeated breaker operation requires escalation.

7. Inspect for Environmental or Ventilation Problems

Confirm ventilation openings are not blocked.

Remove external stored items restricting airflow.

Check for excessive room heat or recent HVAC failure.

Look for dust accumulation on accessible vents.

Do not remove panels to clean internal components.

Confirm required clearances around the sterilizer are maintained.

Expected outcome: The sterilizer has unobstructed airflow and a suitable environment. If correcting an external blockage resolves the issue, continue with complete test-cycle verification.

8. Disconnect Nonessential External Peripherals

When the sterilizer is idle:

Inspect connected printers, scanners, USB devices, and network accessories.

Disconnect recently added nonessential peripherals.

Check for damaged cables or liquid contamination.

Restart the sterilizer using its normal procedure.

Reconnect approved peripherals one at a time after stable operation is confirmed.

Expected outcome: The sterilizer remains powered without the suspect peripheral. If the shutdown follows one accessory, remove that accessory from service.

9. Perform a Controlled Restart

After facility power and connections are confirmed:

Start the sterilizer according to normal procedures.

Observe the complete startup sequence.

Record any fault or self-test message.

Confirm the display, door status, sterilant status, and peripherals initialize normally.

Stop if the unit restarts again, makes abnormal sounds, or develops heat or odor.

Expected outcome: The sterilizer reaches a stable ready state without restarting.

10. Run an Approved Test Cycle

Do not begin with a clinical load.

Run the facility-approved verification or empty test cycle.

Observe whether the shutdown repeats at the same phase.

Monitor external power stability and physical indicators.

Confirm the full cycle record is produced.

Stop further testing after one repeated unexpected shutdown.

Expected outcome: The sterilizer completes the test cycle without power loss, restart, alarm, or missing data.

11. Verify Recovery and Record Integrity

Confirm:

Expected outcome: The sterilizer’s operational and documentation functions remain reliable following the event.

If the Problem Persists

If facility power, branch circuit, external connections, ventilation, environment, and peripherals have been checked and the sterilizer still shuts down or restarts, common external causes have been ruled out.

The remaining cause may involve an internal power supply, control system, wiring connection, thermal protection circuit, electrical load, software, or another internal component.

The sterilizer should be:

Do not repeatedly restart the sterilizer, reset tripping protection, or run additional clinical loads. Complete electrical safety, operational, and sterilization-process verification after repair.

Knowing when to stop external troubleshooting is proper troubleshooting.

Clinical Use Tip

Every load interrupted by a power loss must be fully reprocessed, even when the sterilizer restarts and displays a normal ready screen.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"Sterile Processing reported that the V-PRO restarted during conditioning and the cycle was aborted."

Cause

What was observed during troubleshooting.

Example:
"Clinical Engineering and Facilities found a loose connection at the approved power receptacle that caused intermittent loss of supply power."

Resolution

What action was taken.

Example:
"Facilities repaired the receptacle, and Clinical Engineering verified stable startup, a complete test cycle, accurate records, and normal door operation."

Helpful Details to Include (If Known)

Final Thought

Treat every shutdown as both a load-validity and electrical-safety concern. Rule out facility power, external connections, circuit events, airflow, and peripherals before suspecting internal failure, and stop testing when the event repeats.

That is successful troubleshooting.

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