CONMED AirSeal iFS

Preventive Maintenance or Electrical Safety Test Failure

On this page

Asset Type

Surgical Smoke Evacuator

Manufacturer

CONMED

Model

AirSeal iFS

What This Guide Helps With

Troubleshoots PM or electrical-safety failures by verifying test setup, accessories, power configuration, physical condition, test equipment, and documented requirements.

Step-by-Step Troubleshooting

1. Keep the Device Out of Clinical Service

If the AirSeal iFS fails a required preventive-maintenance or electrical-safety test, do not return it to clinical use until the failure is understood and appropriately resolved.

Expected outcome: A device with an unresolved required test failure remains controlled by Clinical Engineering.

2. Identify the Exact Failed Test

Record the specific failed inspection or test and the observed result.

Determine whether the failure involves:

Do not describe the result only as "PM failed."

Expected outcome: The failed requirement is clearly identified and reproducible.

3. Verify the Correct Procedure and Test Setup

Confirm the test was performed using the current approved procedure, correct equipment configuration, and appropriate test equipment.

Verify the analyzer or test instrument is within its required calibration status according to facility policy.

Do not invent acceptance limits or substitute limits from unrelated equipment.

Expected outcome: The test result is based on a valid procedure and valid test setup.

4. Perform a Thorough External Inspection

Inspect the:

Look for cracks, looseness, contamination, heat damage, exposed conductors, or evidence of fluid intrusion.

Expected outcome: Any visible condition contributing to the failed PM is identified before deeper investigation.

5. Verify AC Power and Grounding Environment

Use an approved method to verify that the test receptacle and test setup are suitable.

A faulty receptacle, adapter, extension device, or incorrect analyzer connection can produce misleading results.

Expected outcome: The facility power and test connection are confirmed appropriate.

6. Remove Unnecessary External Equipment From the Test

Disconnect nonessential accessories, external interfaces, or cart-mounted equipment when the approved test procedure permits.

If the system is normally tested with specified accessories attached, follow that documented configuration instead.

Expected outcome: The AirSeal iFS is tested in the correct configuration without unrelated external equipment affecting the result.

7. Repeat the Failed Test Once After Correcting Setup Issues

If an external setup problem is found, correct it and repeat only the relevant failed test using the approved method.

Do not repeatedly test until a marginal result happens to pass.

Expected outcome: The repeated result is stable and confirms whether the failure was caused by setup or remains associated with the device.

8. Perform Applicable Functional Checks

If the electrical-safety result is acceptable after correcting an external issue, continue the remaining required PM functional checks.

Verify startup, controls, alarms, relevant AirSeal functions, and accessory operation as required by the approved procedure.

Expected outcome: All required PM functions are completed successfully.

9. Document the Final Verification

Record the original failed test, the cause identified, corrective action, repeat-test result, and final PM status.

Do not document "passed" without preserving the fact that a failure was initially found and corrected.

Expected outcome: The work order clearly demonstrates why the equipment is considered safe for return to service.

10. Escalate a Confirmed Device Failure

If the same required electrical-safety or functional test continues to fail with verified test equipment and setup, stop troubleshooting at the external level.

Expected outcome: The device remains out of service and is referred for repair rather than being released on the basis of normal appearance or operation.

If the Problem Persists

Common setup and external causes have been ruled out. A persistent PM or electrical-safety failure may involve an internal electrical, mechanical, pneumatic, sensing, protective-earth, software, or other service-level condition depending on the test that failed.

The device should be:

After repair, repeat the failed test and any other required return-to-service testing before clinical release.

Knowing when to stop external troubleshooting and escalate is proper troubleshooting.

Clinical Use Tip

A device that appears to function normally should not be returned to use after a required safety test failure until that failure has been resolved and verified.

Work Order Documentation (CCR Method)

CCR = Complaint, Cause, Resolution

Complaint

What was reported by the clinical staff.

Example:
"The CONMED AirSeal iFS failed an electrical-safety test during scheduled preventive maintenance."

Cause

What was observed during troubleshooting.

Example:
"Clinical Engineering found that the initial test was performed through a defective external power adapter in the test setup rather than directly from the verified test receptacle."

Resolution

What action was taken.

Example:
"Removed the defective adapter, repeated the electrical-safety test using the approved setup, completed functional PM checks successfully, and returned the unit to service."

Helpful Details to Include (If Known)

Final Thought

A PM failure should trigger investigation, not automatic parts replacement and not repeated testing until a pass occurs. Verify the procedure, test setup, external condition, and equipment first; then escalate a confirmed device failure and document the complete CCR trail.

That is successful troubleshooting.

Related Guides

Was this guide helpful?

Don't see a guide you need?

Suggest a Guide