Getinge ROTAFLOW II

Battery Not Charging or Short Transport Runtime

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Asset Type

Extracorporeal Membrane Oxygenation (ECMO) System

Manufacturer

Getinge

Model

ROTAFLOW II

What This Guide Helps With

Troubleshoots charging failure and reduced battery runtime involving AC power, charging status, battery condition, connectors, storage, and external operating conditions.

Step-by-Step Troubleshooting

1. Protect the Patient Before Evaluating Battery Operation

Do not intentionally remove AC power from a patient-supporting ECMO system to test battery runtime. If transport backup power is questionable, use a verified alternate transport power plan and follow the ECMO team's backup procedure.

Expected outcome: ECMO support does not depend on an unverified battery.

2. Confirm the Battery Complaint

Determine whether:

Document AC status, displayed battery indication, and conditions when the problem occurred.

Expected outcome: The battery problem is clearly distinguished from a general console power problem.

3. Verify the AC Power Source

Confirm the wall outlet or approved transport power source is functional. Inspect the external power cord, plug, and accessible inlet for damage.

Expected outcome: Reliable AC power reaches the system and charging status can be evaluated correctly.

4. Verify Charging Indications

Observe the console's normal battery and charging indications while connected to verified AC power.

Allow the system to remain connected under normal charging conditions as appropriate to determine whether the status changes.

Expected outcome: The system recognizes external power and indicates charging appropriately. If a poor power connection caused the issue, correct it and continue verification.

5. Inspect External Battery-Related Connections

Where battery components or connections are externally accessible without disassembly, inspect for:

Do not use a damaged, swollen, leaking, or overheated battery.

Expected outcome: No unsafe battery condition is present and accessible connections are secure.

6. Review Recent Use and Storage Conditions

Determine whether the device:

These factors may explain a temporarily low charge or degraded battery condition without establishing the exact internal cause.

Expected outcome: Charging and runtime observations are interpreted in the correct operational context.

7. Perform an Approved Battery Functional Check

With the system removed from patient use, perform the manufacturer- or facility-approved battery evaluation using appropriate test conditions.

Do not create an improvised transport-runtime test on clinical equipment supporting a patient.

Expected outcome: Battery performance is adequate for the approved test or the battery clearly fails the applicable evaluation.

8. Compare With a Known-Good Battery When Applicable

If the battery is an approved field-replaceable component and qualified personnel are authorized to exchange it, compare operation with a known-good compatible battery following the appropriate procedure.

Do not open the unit or access internal batteries unless authorized.

Expected outcome: Normal charging and runtime with a known-good battery isolates the original battery as the likely service component.

9. Perform Final Functional Verification

After correction, verify:

Expected outcome: Battery backup is reliable under approved test conditions. Troubleshooting can stop.

10. Escalate Persistent Charging or Runtime Failure

If verified AC power, appropriate charging time, secure accessible connections, and approved battery testing do not produce acceptable operation, remove the system from service.

Expected outcome: Battery, charging-system, power-management, or internal electronic issues are referred for qualified evaluation.

If the Problem Persists

External AC power, charging conditions, accessible connections, storage history, and approved battery checks have been completed. Remaining possibilities include battery degradation, charging circuitry, internal power distribution, or battery-management electronics.

The device should be:

Following corrective action, complete charging, battery backup, alarm, and full system functional testing before return to service.

Knowing when to stop external troubleshooting is proper troubleshooting.

Clinical Use Tip

Confirm transport power capability before moving an ECMO patient; transport is not the time to discover that the console battery cannot sustain reliable operation.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"ECMO staff reported the ROTAFLOW II battery was not charging while the console was staged for transport."

Cause

What was observed during troubleshooting.

Example:
"Clinical Engineering found the external AC power cord was not fully seated at the console power inlet."

Resolution

What action was taken.

Example:
"Secured the power connection, confirmed normal charging indication and approved battery operation, completed functional checks, and returned the system to service."

Helpful Details to Include (If Known)

Final Thought

Maintain safe ECMO backup power, verify the external charging path before condemning the battery, test backup operation under controlled conditions, and escalate any unreliable transport-power system.

That is successful troubleshooting.

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