Getinge Volista

Unexpected Shutdown, Freeze, or Restart

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Asset Type

Surgical Light

Manufacturer

Getinge

Model

Volista

What This Guide Helps With

Troubleshoots intermittent Volista shutdowns, freezes, or restarts associated with power, controls, connections, environmental conditions, movement, or service-level faults.

Step-by-Step Troubleshooting

1. Protect the Patient Immediately

If the surgical light shuts down, freezes, or restarts during use, provide verified alternate surgical illumination before continuing troubleshooting. Do not repeatedly test an unstable system while a procedure depends on it.

Expected outcome: Patient care continues with dependable lighting and the affected Volista is removed from clinical dependence.

2. Capture the Event Details

Ask staff what happened immediately before the event. Record whether illumination stopped completely, controls froze while the light remained on, the display restarted, one head was affected, or the whole system cycled.

Expected outcome: The failure mode and affected portion of the installation are clearly defined.

3. Check for Obvious Safety Concerns

Inspect for unusual heat, burning odor, smoke, fluid intrusion, sparking, physical damage, or abnormal noise. If any are present, disconnect or isolate power according to facility safety procedures and do not re-energize the system.

Expected outcome: No immediate electrical or physical hazard is present, or the equipment is removed from service without further testing.

4. Verify Facility Power

Check normal power availability and investigate whether the event coincided with a facility outage, breaker event, emergency-power transfer, or work on the electrical system. Coordinate with Facilities where necessary.

Expected outcome: Facility power instability is identified or ruled out.

5. Inspect Accessible Power and Control Connections

Inspect accessible external cables, connectors, wall controls, and interfaces for looseness, damage, or strain. Pay attention to any connection that may have been disturbed by cleaning, construction, or recent service.

Expected outcome: Accessible connections are secure and undamaged.

6. Determine Whether Movement Triggers the Failure

With the device safely out of clinical use, move the light through its normal positioning range while observing operation. Do not disassemble joints or internal wiring paths.

Expected outcome: The system remains stable throughout movement. If shutdown or restart occurs reproducibly during movement, stop testing and remove it from service.

7. Check Environmental Conditions

Confirm that ventilation openings are unobstructed and that the system is not exposed to unusual heat, moisture, or environmental conditions. Do not open internal housings to investigate thermal components.

Expected outcome: No correctable external environmental condition explains the event.

8. Perform a Controlled Normal Restart

If no safety concerns are present, restart the system using normal approved controls and observe whether it initializes and remains stable.

Expected outcome: The system starts normally and remains operational. A single recovery is not sufficient if the original failure was intermittent.

9. Reproduce Normal Operation

Operate controls, intensity adjustment, positioning, and any clinically used accessories long enough to determine whether the failure recurs under the reported conditions.

Expected outcome: Operation remains stable with no freezes, shutdowns, or unintended restarts. If the external cause was identified and stability is verified, troubleshooting can stop.

10. Escalate an Intermittent Unexplained Failure

If the system freezes, shuts down, or restarts again without a verified external cause, remove it from service even if it subsequently appears normal.

Expected outcome: Intermittent unreliability is treated as a service issue rather than cleared without evidence.

If the Problem Persists

Common facility-power, connection, movement-related, control, and environmental causes have been ruled out. The remaining issue may involve internal power electronics, wiring, control electronics, software, thermal protection, or another service-level fault.

Remove the system from service, label it Out of Service, and arrange qualified repair or technical evaluation using current Getinge documentation and approved test equipment. Do not attempt internal board-level troubleshooting or unauthorized software/configuration changes.

Before return to service, verify repeated stable startup, sustained illumination, controls, positioning, and all clinically used functions. Knowing when to stop external troubleshooting is proper troubleshooting.

Clinical Use Tip

An intermittent surgical light that works again after restarting is not automatically safe to return to service; the cause and stability must be verified.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"OR staff reported that the Volista unexpectedly restarted when the light was repositioned."

Cause

What was observed during troubleshooting.

Example:
"Clinical Engineering reproduced the event during arm movement and found an accessible external connection under strain."

Resolution

What action was taken.

Example:
"The connection and cable routing were corrected within approved external service limits, repeated movement and lighting tests remained stable, and the system was returned to service."

Helpful Details to Include (If Known)

Final Thought

Treat intermittent loss of surgical illumination seriously, capture the circumstances, verify external power and connections first, require stable repeat testing, and escalate unexplained recurrence.

That is successful troubleshooting.

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