ICU Medical Plum Duo: troubleshooting and error codes
The ServiceForge knowledge base holds 116 documented symptoms for the ICU Medical Plum Duo, with 166 ranked causes, 141 diagnostic checks with test points and expected values, and 93 error codes. Each symptom below shows its causes and the first check; the rest is one connection away. Connect ServiceForge to your AI
Symptoms
Upstream occlusion test fails caution
Upstream occlusion detection test does not complete successfully
Ranked causes
- 1. Closed upstream clamp (common)
- 2. Cassette not properly primed (common)
- 3. Defective cassette (occasional)
- 4. Dirty sensor pin (occasional)
- 5. Defective APP PWA (rare)
Verify upstream clamp open
- Test point
- upstream clamp position
- Expected
- Clamp in open position
6 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Downstream occlusion test fails caution
Downstream occlusion detection test does not complete successfully
Ranked causes
- 1. Cassette not properly primed (common)
- 2. Defective cassette (occasional)
- 3. Dirty sensor pin (occasional)
- 4. Defective APP PWA (rare)
Verify cassette priming
- Test point
- cassette fluid level
- Expected
- Cassette fully primed with no air bubbles
1 more check with pass and fail actions, 5 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Pole clamp does not hold infusion pump securely on IV pole patient safety
Infusion pump slides on IV pole when clamp is fully tightened; pump not held firmly in place
Ranked causes
- 1. Rubber pad missing from pole clamp extrusion (occasional)
- 2. Plastic shaft tip damaged or missing (occasional)
- 3. Pole clamp assembly damaged or worn (occasional)
- 4. Pole clamp assembly loose on rear housing (common)
Visually inspect pole clamp assembly attachment to rear housing
- Test point
- Pole clamp assembly fasteners
- Expected
- Securely attached, no movement or looseness
3 more checks with pass and fail actions, 4 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Unable to connect to ISMS
Infusion pump cannot establish connection to ICU Medical ISMS server
Ranked causes
- 1. Inappropriate device name configured (occasional)
- 2. ISMS port number not added to ISMS hostname or IP (occasional)
- 3. Server certificate not properly installed (occasional)
- 4. ISMS Host/IP mismatch or incorrect URL format (occasional)
Verify device name setting
- Test point
- Pump configuration
- Expected
- Appropriate device name configured
3 more checks with pass and fail actions, 4 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Unrestricted flow patient safety
Infusion pump fails unrestricted flow test or fluid flows without pump delivering it
Ranked causes
- 1. Cassette not properly seated (common)
- 2. Defective cassette (occasional)
- 3. Defective or dirty valve pins (occasional)
- 4. Regulator closer not properly seated (rare)
Verify cassette seating
- Test point
- cassette position
- Expected
- Cassette fully seated and locked
2 more checks with pass and fail actions, 7 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Ambient light sensor not adjusting screen brightness
Screen does not dim automatically when ambient light is blocked; brightness adjustment fails or does not respond within 2-5 seconds after covering sensor behind logo
Ranked causes
- 1. Backlight LED failure (occasional)
- 2. Bridge Flex Cable damage or disconnection (occasional)
- 3. Ambient light sensor (Power Button Assembly) malfunction (occasional)
Verify screen brightness adjusts automatically when sensor is covered
- Test point
- Ambient light sensor location behind ICU Medical logo letter 'd'
- Expected
- Screen dims after 2-5 seconds when sensor is covered
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Delivery accuracy test fails patient safety
Infusion pump does not deliver fluid at specified rate or volume
Ranked causes
- 1. Set not properly primed (common)
- 2. Damaged or faulty cassette (occasional)
- 3. Defective infusion mechanism assembly (rare)
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Downstream air-in-line test fails caution
Downstream air detection does not function during PVT
Ranked causes
- 1. Defective downstream test cassette (occasional)
- 2. Dirty sensors (occasional)
- 3. Defective APP PWA (rare)
4 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Power cord or retainer damaged high voltage
AC power cord, retainer, or strap shows signs of damage, arcing, burn marks, melting, bent prongs, or physical breakage
Ranked causes
- 1. Physical damage from handling or wear (occasional)
- 2. Retainer broken or missing parts (occasional)
- 3. Strap damage (occasional)
Disconnect and power down pump
- Test point
- AC mains and POWER button
- Expected
- Device powered off after holding POWER button 5 seconds minimum
5 more checks with pass and fail actions, 3 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Pressure sensor or control pins damaged or contaminated
Line 1/2 pins, Upstream/Downstream pressure pins, or Inlet/Outlet valve pins are broken, chipped, or have dried fluid buildup around them; cassette presence diaphragm is damaged, torn, or missing
Ranked causes
- 1. Pin damage from impact or wear (rare)
- 2. Dried fluid accumulation on pins (common)
- 3. Cassette presence diaphragm torn, damaged, or missing (rare)
Inspect all control pins for damage
- Test point
- Line 1/2 pins, Upstream/Downstream pressure pins, Inlet/Outlet valve pins
- Expected
- All pins intact, no breaks or chips
2 more checks with pass and fail actions, 3 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Unable to update Drug Library patient safety
Drug Library update fails, preventing configuration changes
Ranked causes
- 1. Public certificate not configured (common)
- 2. No connectivity to Lifeshield (occasional)
- 3. Persistent error requiring service (occasional)
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Upstream air-in-line test fails caution
Upstream air detection does not function during PVT
Ranked causes
- 1. Defective upstream test cassette (occasional)
- 2. Dirty sensors (occasional)
- 3. Defective APP PWA (rare)
4 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Web Config is not accessible
Unable to reach the Web Config interface for the infusion pump
Ranked causes
- 1. Infusion pump not in Biomed mode or Web Config disabled (common)
- 2. CE not connected over Wi-Fi (common)
- 3. Incorrect Web Config URL format (occasional)
Verify pump is in Biomed mode and Web Config enabled
- Test point
- Pump display and configuration settings
- Expected
- Biomed mode active, Web Config enabled
2 more checks with pass and fail actions, 3 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Alarm loudness test fails
Speaker does not produce audible alarm at required loudness level
Ranked causes
- 1. Defective speaker assembly (rare)
- 2. Defective CPU (rare)
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Artifacts on ECG, EMG, or EEG monitoring patient safety
Abnormal waveforms or signals appearing on voltage-sensing monitoring equipment (ECG, EMG, EEG machines) that vary at a rate associated with infusion rate
Ranked causes
- 1. Electronic noise generated by infusion pump (common)
- 2. Loose or defective connections to monitoring electrode (occasional)
Verify if artifact is caused by infusion pump
- Test point
- Monitoring equipment display
- Expected
- Artifact disappears when infusion pump is not delivering fluid
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery not charging when connected to AC power caution
Battery does not charge or charging is reduced when pump is plugged into AC mains power despite State of Charge being ≤95%.
Ranked causes
- 1. Battery temperature outside charging threshold (below 0°C or above 45°C) (occasional)
- 2. Reduced charging if battery temperature between 0°C and 10°C (occasional)
Verify battery temperature is within safe charging range (0–45°C)
- Test point
- Battery thermal sensor or device ambient temperature
- Expected
- Battery temperature 0°C < T < 45°C for normal charging, or 0°C < T < 10°C for reduced charging
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Cassette alarm test fails
Cassette alarm test does not complete successfully during PVT
Ranked causes
- 1. Cassette not properly seated (common)
- 2. Defective cassette (occasional)
Verify cassette seating
- Test point
- cassette position
- Expected
- Cassette fully seated
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Cassette door damaged or stiff
Cassette door has chips or damage, or moves stiffly when opening/closing; door does not open smoothly
Ranked causes
- 1. Physical damage to cassette door (occasional)
- 2. Debris or dried fluid buildup on infusion mechanism (common)
Inspect cassette door for chips or damage
- Test point
- Cassette door surface
- Expected
- No damage or chips present
1 more check with pass and fail actions, 3 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Door lever damaged or stiff
Door lever has damage, is difficult to move, or does not operate smoothly between OPEN and CLOSED positions
Ranked causes
- 1. Physical damage to door lever (occasional)
- 2. Debris or dried fluid on lever mechanism (common)
Inspect door lever for damage
- Test point
- Door lever body
- Expected
- No damage or cracks visible
2 more checks with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Door roller does not spin smoothly or is obstructed
Door roller wheel does not spin freely with finger touch, is stuck, or has bent/loose mounting pin or retaining ring
Ranked causes
- 1. Door roller damaged or misaligned (occasional)
- 2. Retaining ring not seated or pin bent (occasional)
Spin door roller by hand
- Test point
- Door roller wheel
- Expected
- Roller spins smoothly with light finger touch
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Downstream occlusion pressure reading incorrect at 10 psi patient safety
Digital Pressure Meter does not display 10 psi (517 mmHg) ±3 psi tolerance when downstream occlusion alarm is triggered during second test at 10 psi setting
Ranked causes
- 1. Downstream pressure sensor calibration drift or malfunction at higher pressure (occasional)
- 2. Digital Pressure Meter accuracy degradation at elevated pressure (occasional)
Adjust downstream pressure limit to 10 psi (517 mmHg) in Clinical Settings
- Test point
- Clinical Settings > Downstream Pressure > Occlusion Alarm Limit field
- Expected
- Pressure limit adjusted to 10 psi (517 mmHg)
2 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Downstream occlusion pressure reading incorrect at 6 psi patient safety
Digital Pressure Meter does not display 6 psi (310 mmHg) ±3 psi tolerance when downstream occlusion alarm is triggered during test at 6 psi setting
Ranked causes
- 1. Downstream pressure sensor calibration drift or malfunction (occasional)
- 2. Digital Pressure Meter calibration error or malfunction (occasional)
Verify downstream pressure limit is set to 6 psi (310 mmHg) in Clinical Settings
- Test point
- Clinical Settings > Downstream Pressure > Occlusion Alarm Limit field
- Expected
- Pressure limit displays as 6 psi (310 mmHg)
3 more checks with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Drug library update activation delayed or not automatic patient safety
Updated drug library does not activate immediately or user is not prompted with activation option as expected
Ranked causes
- 1. Active therapy data present when update downloaded (common)
- 2. No active therapy data but update not auto-activated (rare)
Verify presence of active therapy data
- Test point
- Therapy screen/programmed therapy status
- Expected
- No active or programmed therapy
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Drug library update fails to download patient safety
Update process encounters an error and cannot complete; message displayed indicates whether pump remains usable
Ranked causes
- 1. Loss of connectivity to LifeShield (common)
- 2. Invalid or missing certificate information (occasional)
Verify connectivity to LifeShield system
- Test point
- Wireless/network connection status
- Expected
- Connected to LifeShield
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Electrical safety test high voltage
Verify leakage current, earth resistance, and chassis ground meet safety specifications using safety analyzer under normal and single fault conditions.
Ranked causes
- 1. Leakage current exceeds specification (unknown)
- 2. Chassis ground resistance exceeds specification (unknown)
Connect safety analyzer to power source
- Test point
- Safety analyzer inlet
- Expected
- Safety analyzer powered on
8 more checks with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Housing cracked, chipped, gouged, stained, or discolored patient safety
Front, rear, or bottom housing has visible cracks, chips, gouges, significant stains, or discoloration
Ranked causes
- 1. Physical impact or damage (occasional)
- 2. Staining or discoloration of housing (occasional)
Inspect front and rear housings for structural damage
- Test point
- Front housing surface, rear housing surface
- Expected
- No cracks, chips, or gouges present
3 more checks with pass and fail actions, 6 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Loss of communication with LifeShield software patient safety
Plum Duo loses communication with LifeShield Infusion Safety Software Suite; LifeShield icon not displayed in pump
Ranked causes
- 1. Low Wi-Fi connectivity (common)
- 2. Disruption between LifeShield software and hospital network (occasional)
Verify LifeShield icon display status in pump
- Test point
- pump display
- Expected
- LifeShield icon present when communication active
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Self test fails
Infusion pump fails self-test on startup
Ranked causes
- 1. Cassette not properly installed (common)
- 2. Defective CPU PWA (rare)
Verify cassette installation
- Test point
- cassette seating
- Expected
- Cassette fully seated and locked
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Suspected cybersecurity event or threat patient safety
External RF sources or electromagnetic disturbance affecting essential performance; wireless connectivity interrupted; battery icon shows incorrect charge/discharge status
Ranked causes
- 1. External RF sources or electromagnetic interference (unknown)
- 2. Wireless connectivity interference (occasional)
Verify wireless connectivity recovery time
- Test point
- wireless connection status
- Expected
- connection restored within 50 seconds after interference removed
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Unable to update infusion pump settings patient safety
Infusion pump settings update fails, preventing configuration changes
Ranked causes
- 1. No connectivity to Lifeshield (common)
- 2. Persistent error requiring service (occasional)
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Worn or defective external pump components patient safety
Signs of wear on accessories, broken connections, damaged cable assemblies, or other defective external parts detected during inspection or after repair/cleaning
Ranked causes
- 1. Normal wear or age (common)
- 2. Damage from prior repair or cleaning (occasional)
Visually inspect all external pump components
- Test point
- Accessories, connections, cable assemblies
- Expected
- No visible wear, breaks, damage, or defects
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Abnormal operation in stacked or adjacent configuration patient safety
Infusion pump not operating normally when positioned adjacent to or stacked with other equipment
Ranked causes
- 1. Electromagnetic interference from adjacent/stacked equipment (unknown)
Verify pump normal operation in stacked/adjacent configuration
- Test point
- Display, alarms, infusion delivery
- Expected
- All functions operate normally as in standalone configuration
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
AC ON LED not illuminated when connected to AC power
Green AC ON indicator LED does not light when infusion pump is plugged into AC mains power
Ranked causes
- 1. CPU PWA defective (rare)
Connect power cord to AC mains and observe AC ON LED status
- Test point
- AC ON LED on infusion pump front panel
- Expected
- Green LED illuminated steadily when plugged into AC power
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Alarm condition occurs during self test patient safety
Alarm condition triggered during SYSTEM SELF TEST IN PROGRESS execution
Ranked causes
- 1. Unspecified self test failure (unknown)
Cycle power and repeat self test
- Test point
- Device power and self test function
- Expected
- Self test completes without alarm
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
ALS driver communication failure
Alert E462 displays; communication failure with ALS driver detected
Ranked causes
- 1. ALS driver communication failure (unknown)
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery communication lost caution
Battery alert E465 displays; communication to battery has been lost
Ranked causes
- 1. Battery communication lost (occasional)
5 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery has reduced capacity patient safety
Replace Battery condition registered, BATTERY NEEDS SERVICE alarm appears, audio indicator activates and persists over power cycles
Ranked causes
- 1. Battery degradation beyond acceptable threshold (common)
Verify battery charge level
- Test point
- Battery display
- Expected
- 100% charge
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery icon displays incorrect charge or discharge status
Battery charge level indicator shows inaccurate status
Ranked causes
- 1. Electromagnetic interference affecting battery indicator (occasional)
Monitor battery indicator recovery time
- Test point
- Battery icon display
- Expected
- Correct battery status displayed within 6 seconds after interference removed
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery leakage or degradation during extended storage caution
Battery may leak or degrade if pump stored for extended period with battery installed.
Ranked causes
- 1. Battery left installed in stored pump over extended period (occasional)
Confirm pump will be stored for extended period (determine storage duration)
- Test point
- Storage plan or schedule
- Expected
- If storage > 30 days (or per facility policy), remove battery.
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery level insufficient for update
Alert N702 displays; battery level is not sufficient for resource update or device settings update
Ranked causes
- 1. Battery level below 50% (common)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery low alarm timing inaccurate or battery state of health not understood
Low battery alarm triggers at incorrect time; battery condition monitoring is inaccurate
Ranked causes
- 1. Battery reconditioning not performed within 24 months (common)
Verify battery reconditioning has been performed within last 24 months
- Test point
- Service record documentation
- Expected
- Battery reconditioning date within 24 months
1 more check with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery operating outside specified temperature or storage conditions caution
Battery used or stored outside acceptable range (0–45°C), risking shortened lifespan or damage.
Ranked causes
- 1. Battery exposed to temperature below 0°C or above 45°C during operation or storage (occasional)
Verify storage and operating environment temperature is within 0–45°C
- Test point
- Ambient temperature where pump/battery is kept
- Expected
- Temperature maintained between 0°C and 45°C continuously
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery temperature out of range caution
Battery alert E464 displays; battery reporting too high or too low temperature
Ranked causes
- 1. Battery temperature too high or too low (common)
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Bottom housing or battery cover assembly screws loose or missing
Assembly screws on bottom housing or battery cover are not tight or are absent
Ranked causes
- 1. Vibration or handling during use or transport (occasional)
Verify bottom housing assembly screws
- Test point
- Four assembly screws on bottom housing
- Expected
- All four screws present and tight
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Broken downstream pin detected
Pump malfunction alarm E458 displays; broken downstream pin detected during cassette test
Ranked causes
- 1. Broken downstream pin (unknown)
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Delivery accuracy patient safety
Periodic verification that pump delivers accurate volume over programmed time interval at specified rates.
Ranked causes
- 1. Periodic maintenance requirement (common)
Ensure graduated cylinder is completely dry before testing each channel
- Test point
- 25 mL graduated cylinder
- Expected
- Interior dry, no residual fluid
1 more check with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Downstream occlusion pressure threshold patient safety
Service test to verify downstream occlusion detection triggers at correct pressure with DPM connected and 3-way stopcock setup
Ranked causes
- 1. Pressure threshold calibration verification required (common)
Wait for DPM pressure stabilization
- Test point
- DPM pressure gauge
- Expected
- Pressure stable after 10 seconds
2 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Cassette alarm not triggering during cassette test patient safety
CASSETTE CHECK FAILURE alarm does not flash or audible alarm does not sound during cassette testing with empty run-in cassette inserted
Ranked causes
- 1. Cassette sensor malfunction or detection failure (occasional)
Insert empty (not primed) run-in cassette and close cassette door
- Test point
- Cassette door opening and insertion
- Expected
- CASSETTE TESTING IN PROGRESS message appears on display
2 more checks with pass and fail actions are in ServiceForge. Connect ServiceForge to your AI
CDL required flag issue with missing or invalid drug library patient safety
Alarm indicates CDL (Configured Drug Library) required flag not set and either CDL is not present or fails integrity checks
Ranked causes
- 1. CDL missing or integrity failure (common)
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
CPU and RTC clock frequencies mismatch
Pump malfunction alarm E444 displays; CPU and RTC clock frequencies mismatch during power on self test for PMC
Ranked causes
- 1. CPU and RTC clock frequencies mismatch (unknown)
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Damage or degradation from use of unapproved charger high voltage
Use of non-designated battery charger causes electrical/mechanical damage, heat generation, leakage, or safety degradation.
Ranked causes
- 1. Unapproved or non-designated charger used to charge battery (rare)
Confirm designated Plum Duo AC power supply being used for charging
- Test point
- Power supply model/part number and connection to pump
- Expected
- Designated ICU Medical Plum Duo AC power supply connected; no external chargers or adapters
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Damaged infusion pump found after shipment patient safety
External damage visible on shipping container or pump housing, worn accessories, broken connections, or damaged cable assemblies
Ranked causes
- 1. Shipping or handling damage (occasional)
Inspect shipping container for external damage
- Test point
- Entire exterior of container
- Expected
- No visible damage, dents, or crushing
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Delivery accuracy test verification patient safety
Verify infusion pump delivers correct volume over time. Test performed on both channels (L1, L2, R1, R2) using graduated cylinder collection.
Ranked causes
- 1. Pumping chamber fatigue after repeated tests (occasional)
Attach 18-gauge blunt cannula to downstream tubing end
- Test point
- Downstream tubing cannula
- Expected
- Cannula securely attached, lines primed
- Tools
- 18-gauge blunt cannula
3 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
DEPLETED BATTERY alarm and pump shutdown patient safety
Continuous alarm tone sounds; DEPLETED BATTERY message displays; pump stops infusion and automatically powers off after approximately 3 minutes.
Ranked causes
- 1. Battery fully discharged after VERY LOW BATTERY alarm ignored or unaddressed (occasional)
Assess pump power state after depletion event
- Test point
- Pump display and power indicators
- Expected
- Pump OFF; no infusion active; alarm sounding or device in shutdown state after ~3 minutes
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Display backlight not adjustable or auto-brightness not functional
Backlight intensity cannot be changed; auto-brightness feature not working; display brightness cannot be adjusted
Ranked causes
- 1. Backlight control hardware or firmware issue (rare)
Access Settings menu and select BACKLIGHT option
- Test point
- Pump Settings - Backlight Level screen
- Expected
- Backlight Level screen displayed with slider and auto-brightness options
3 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Display scratched, broken, unclear, or has defective pixels patient safety
LCD display shows scratches, cracks, broken areas, defective pixels, or is not clearly legible; information not readable
Ranked causes
- 1. Display module defective or damaged (occasional)
Observe LCD display for defective pixels during self-test with ICU Medical logo
- Test point
- Display screen during self-test
- Expected
- No defective pixels visible; solid light blue background
2 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Display test fails
Display assembly does not respond or shows no output during PVT
Ranked causes
- 1. Defective display assembly (rare)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Downstream air-in-line alarm not triggering patient safety
Alarm should sound and display should blink red before 1 mL fluid is delivered when air is detected downstream
Ranked causes
- 1. Air detection sensor not functioning or cassette not primed correctly (common)
Start infusion with downstream air test cassette
- Test point
- Activity line indicator
- Expected
- PUMPING with start tone and green background screen
1 more check with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Downstream occlusion alarm not triggering patient safety
Expected alarm pop-up and audible alarm should appear when downstream occlusion is detected during test with DPM pressure reading at 10 psi ± 3 psi (517 mmHg ± 155 mmHg)
Ranked causes
- 1. DPM pressure not reaching occlusion threshold (10 psi ± 3 psi) (common)
Measure pressure on DPM after 10 second stabilization
- Test point
- DPM
- Expected
- 10 psi ± 3 psi (517 mmHg ± 155 mmHg), ±3 psi
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Downstream pressure pin damaged or bent
Black downstream pressure pin is bent, broken off, or otherwise damaged preventing proper pressure measurement
Ranked causes
- 1. Physical damage to pressure pin (rare)
Inspect downstream pressure pin condition
- Test point
- Downstream pressure pin (black pin)
- Expected
- Pin undamaged, straight, and intact
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
More symptoms
- Drug library activation failed
- Drug library missing or incompatible
- Efuse output out of range
- Electrical safety test fails
- Essential performance affected by electromagnetic disturbance
- Fatal software failures detected
- Fluid shield gap too large or shield not seated properly
- Haptics diagnostic test failure
- Infusion pump does not operate on AC power
- Inter-processor communication timeout
- Invalid date or time value
- Invalid FLASH non-volatile memory type
- Labels illegible or peeling
- LifeShield icon not displayed after update
- LOW BATTERY alarm displays
- Mechanism calibration data CRC error
- Pending software update with patient data present
- Persistent storage write verification error
- Piezo alarm does not sound at battery disconnect
- PMC hardware ID mismatch detected
- POWER button LED not illuminated after pressing power button
- Power button stuck or held
- Pressure sensor fails during delivery
- Programmed bolus conflict with secondary line
- ROM checksum error during CBIT
- RTC time invalid during power on self test
- Rubber pads missing, loose, or peeling
- SLT test failed for PMC
- Software stack memory overflow
- Software update failed
- Software update fails to complete
- Software update in progress
- Software update in progress (N707)
- Software update process takes longer than expected
- Speaker produces no sound or incorrect audio level
- Storage nearly full
- Temperature sensor communication failure
- Touch feedback not functioning
- Touchscreen diagnostics test failure
- Touchscreen keys not responding or input not appearing on display
- Touchscreen verification test fails
- Unable to connect via Wi-Fi
- Unable to upload user-specified wireless certificate
- Unapproved battery not recognized or accepted by pump
- Unrestricted flow test fluid leakage
- Upstream air-in-line alarm not triggering
- Upstream air-in-line detection test
- Upstream occlusion alarm not triggering
- Upstream pressure pin damaged or bent
- VERY LOW BATTERY high priority alarm occurs
- Voltage input too high
- Volume infused and delivery rate mismatch
- Web Config is disabled
- Wireless connectivity interrupted
- Wireless signal icon not displayed
- Wireless signal not appearing on display
56 more symptoms with ranked causes and checks are in ServiceForge. Connect ServiceForge to your AI
Error codes
| Code | Meaning | Trigger | Severity |
|---|---|---|---|
Action Required alarm | System action required from operator | Operational condition requiring user response | warning |
BATTERY NEEDS SERVICE | Battery has reduced capacity beyond acceptable threshold | Battery charge capacity degradation detected during operation | warning |
E300 | Pump malfunction | ADC test error during power on self test and initialization | error |
E302 | Pump malfunction | Voltage current out of range during operation | error |
E303 | Pump audio failure | I2C communication error with audio code or short circuit in speaker driver circuit | error |
E304 | SEND FOR SERVICE | Failure in communication with temperature sensor | warning |
E305 | Pump malfunction | UIC die temperature or UIC silicon temperature exceeds threshold | error |
E306 | Pump audio failure | Piezo buzzer is OFF but sensed ON, or ON but sensed OFF | error |
E310 | Pump malfunction | PMC software reports processor internal die temperature is too high | warning |
E320 | Battery needs service | Average battery current is out of range | warning |
E321 | Battery needs service | After 8 hours charging, battery charge current above expected limit | warning |
E325 | Battery needs service | Battery cell voltage greater than expected limit | warning |
E326 | Battery needs service | Battery not detected | warning |
E329 | Battery needs service | Battery has permanent damage | error |
E330 | Battery needs service | Battery is not recognized | warning |
E331 | Battery needs service | Battery is not recognized | warning |
E332 | Battery needs service | Battery detected short circuit during charge or discharge | error |
E340 | Power cycle pump | Error writing or reading SCP (SPI controller) registers | error |
E341 | Power cycle pump | Critical data verify error | critical |
E343 | Pump malfunction | Downstream air sensor detects liquid with no cassette OR when sensor is turned OFF | error |
E344 | Pump malfunction | Downstream air sensor self test ongoing while cassette inserted OR when sensor turned OFF and out of range | error |
E345 | Pump malfunction | Pressure sensor out of range while sensor OFF | error |
E346 | Pump malfunction | Pressure sensor fails while infusion system in delivery mode | critical |
E347 | Power cycle pump | Watchdog time limit out of range during power on self test | error |
E378 | Pump malfunction | Various I/O valve motor errors | error |
E379 | Pump malfunction | Various L/S valve motor errors | error |
E380 | Pump malfunction | Various plunger motor errors | error |
E430 | Pump malfunction | Upstream air sensor detects liquid with no cassette OR when sensor is turned OFF | error |
E431 | Pump malfunction | Upstream air sensor self test ongoing while cassette inserted OR when sensor turned OFF and out of range | error |
E432 | Pump malfunction | Pressure sensor out of range while sensor OFF | error |
E433 | PUMP MALFUNCTION | Pressure sensor fails while infusion system in delivery mode | error |
E435 | SEND FOR SERVICE | Current date or time is invalid value during read; RTC communication failure | warning |
E436 | POWER CYCLE PUMP | ROM checksum error during CBIT (continuous built in test) | warning |
E437 | POWER CYCLE PUMP | Various fatal software failures including uncontrolled shutdown | critical |
E438 | POWER CYCLE PUMP | Software stack memory overflow | error |
E440 | PUMP MALFUNCTION | Power button pressed and held for 30 seconds or longer while pump not infusing | warning |
E444 | POWER CYCLE PUMP | CPU and RTC clock frequencies mismatch during power on self test for PMC | warning |
E445 | SEND FOR SERVICE | RTC time is invalid value during power on self test | warning |
E446 | POWER CYCLE PUMP | SLT test failed for PMC | warning |
E448 | POWER CYCLE PUMP | Persistent storage write verification error | error |
E449 | PUMP MALFUNCTION | Mechanism calibration data CRC error | error |
E450 | PUMP MALFUNCTION | PMC hardware ID mismatch detected | error |
E451 | PUMP MALFUNCTION | Volume infused and program delivery rate mismatch | error |
E455 | PUMP MALFUNCTION | Invalid FLASH non-volatile memory type | error |
E458 | PUMP MALFUNCTION | Broken downstream pin detected during cassette test | error |
E459 | PUMP MALFUNCTION | Inter-processor communication timeout between PMC and UIC | error |
E460 | PUMP MALFUNCTION | Voltage input VIN_17 too high for over 1 minute sliding window | error |
E461 | PUMP MALFUNCTION | Efuse output out of range | error |
E462 | SEND FOR SERVICE | Communication failure with ALS driver detected | warning |
E464 | BATTERY NEEDS SERVICE | Battery reporting too high or too low temperature | warning |
E465 | BATTERY NEEDS SERVICE | Communication to battery lost | warning |
E466 | POWER CYCLE PUMP | Failure during touchscreen diagnostics test or communication failure | error |
E703 | UPDATE FAILED | Software update failed in PMC1/PMC2, UIC, or CE stages but software is recoverable | error |
N101 | Inactivity timeout - one channel in use, cassette inserted | One channel in use, other has cassette inserted, left idle 5 minutes | info |
N102 | Action required - modal not acknowledged after 15 seconds | Action modal unacknowledged for 15 seconds | warning |
N102 | Action required - no operator action during underlying therapy programming | No operator action for 30 seconds when line programmed during underlying therapy, not confirmed | warning |
N103 | Programming lost - retained delivery parameters corrupted | Corruption of retained delivery parameters detected | error |
N104 | Callback alarm - Line 2 piggyback, Line 1 not resuming, VTBI zero | Line 2 in Piggyback mode, Line 1 not programmed to resume, Line 2 VTBI or multistep becomes 0, Callback enabled | info |
N105 | Callback with delivery stop - infusion halts at step completion | User configures callback and stop; step in multistep, load, bolus or piggyback completes | info |
N159 | Near end of infusion - running therapy within 10 minutes of completion | Active therapy reaches within 10 minutes of completion | info |
N160 | VTBI Complete | Line 2 delivery VTBI = 0 AND line programmed under current CCA AND line 2 has concurrent therapy programmed | info |
N160 | VTBI complete - Line 1 delivery finished under current CCA | Line 1 delivery VTBI = 0 and programmed under current CCA | info |
N160 | VTBI complete - Line 2 piggyback delivery finished | Line 2 delivery VTBI = 0, programmed under current CCA, no delivery on Line 1, Line 2 piggyback configured | info |
N186 | Downstream Occlusion | Downstream occlusion detected with auto-restart off; OR detected with auto-restart on and maximum restarts reached; OR 60 seconds expires without pressure drop below threshold | error |
N187 | Pump High Above Patient | Downstream occlusion detected during delivery due to excessive back pressure (negative detection algorithm) | warning |
N188 | Upstream Occlusion Secondary Line | Upstream occlusion detected on Secondary Line during delivery (negative detection algorithm) | error |
N189 | Upstream Occlusion Secondary Line Peak Detection | Upstream occlusion detected on Secondary Line during delivery (peak detection algorithm) | error |
N192 | Downstream Occlusion Auto Restart | Downstream occlusion detected AND auto-restart configured to on AND maximum auto-restarts not exceeded within last 15 minutes (peak detection algorithm) | warning |
N230 | Upstream Air | Cumulative upstream air detected exceeds air detection threshold (1 mL total or 0.5 mL per line for concurrent delivery) | warning |
N231 | Upstream Air Primary Line Single Bolus | Single air bolus detected at upstream sensor in Primary Line exceeds threshold (0.5 mL or larger) | warning |
N233 | Downstream Air Cumulative | Cumulative air detected at downstream sensor exceeds threshold (0.25 mL out of 4.9 mL fluid) | warning |
N234 | Downstream Air Single Bolus | Single air bolus of 0.1 mL or larger detected at downstream sensor exceeds threshold | warning |
N248 | Very Low Battery | Battery time to empty is at least 15 minutes | warning |
N249 | Door Opened Delayed Start | Cassette door handle opened while in Delayed Start | critical |
N250 | Door Opened During Delivery | Cassette door handle opened while delivering | critical |
N251 | Cassette Check Failure | Faulty cassette, upstream occlusion, or air in cassette detected during cassette initialization | error |
N252 | Depleted Battery | Battery voltage below depleted battery voltage threshold | critical |
N255 | Stopped While Locked | Stop initiated with passcode protected locked touchscreen | warning |
N257 | Pump Audio Failure | I2C communication error with audio codec OR short circuit detected in speaker driver circuit | error |
N258 | SEND FOR SERVICE | Haptics diagnostic test failure during power up | warning |
N56 | Battery does not have sufficient capacity | Battery capacity drops below operational threshold | warning |
N57 | Charger specific malfunction, including charger IC communication | Charger or charging circuit communication failure detected | error |
N58 | Battery charge level is low | Battery charge drops below operational minimum | warning |
N701 | UPDATE FAILED | Drug library activation failed; pump able to rollback to prior custom drug library | error |
N702 | LOW BATTERY | Battery level is not sufficient for resource update or device settings update | info |
N704 | PENDING UPDATE | Patient data present upon pressing power off button when pending update available | warning |
N705 | PROGRAMMED BOLUS | User starts secondary line when bolus actively infusing or stopped on primary or vice versa | info |
N706 | UPDATE IN PROGRESS | Software update is in progress | info |
N707 | UPDATE IN PROGRESS | Software update is in progress | info |
N708 | Storage at least 95% full, cannot write | Pump attempts to write to storage that is at least 95% capacity | error |
N/A | Drug library missing or incompatible and non-recoverable | Drug library required but missing, incompatible, or rollback failed | error |
N/A | CDL integrity check failed or missing | CDL required flag not set and CDL missing or fails integrity checks | error |
Program Inactivity alarm | No action taken within inactivity timeout period | Program interface inactive for extended period | info |
Likely causes and actions for each code are in ServiceForge. Connect ServiceForge to your AI
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ServiceForge knowledge base record. Field-unverified unless technicians confirmed it. A teaching summary of the record, not a service manual. Export 2026-10-14.