Smiths Medical Medfusion 3000: troubleshooting and error codes
The ServiceForge knowledge base holds 74 documented symptoms for the Smiths Medical Medfusion 3000, with 108 ranked causes, 152 diagnostic checks with test points and expected values, and 139 error codes. Each symptom below shows its causes and the first check; the rest is one connection away. Connect ServiceForge to your AI
Symptoms
Pump does not power on
Pump fails to turn on or respond to power button
Ranked causes
- 1. Dead battery (common)
- 2. Main board to interconnect cable disconnected (occasional)
- 3. AC power connection issue (occasional)
- 4. Battery connection issue (occasional)
- 5. Keypad cable disconnected (occasional)
5 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Pump will not turn on or power up
Pump does not respond to power button; no display, no LED indicators, no startup sequence
Ranked causes
- 1. Dead or fully discharged battery; must charge before power-on (common)
- 2. Main PCB to Interconnect PCB ribbon cable loose or disconnected (occasional)
- 3. AC power supply connections loose or missing (occasional)
- 4. Battery connections loose or disconnected (occasional)
- 5. Keypad cable loose or disconnected (occasional)
Connect AC power and charge battery
- Test point
- AC power connection; battery charge status (if readable)
- Expected
- AC power connected; allow 2+ minutes charge time
4 more checks with pass and fail actions, 5 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery does not hold charge
Battery drains quickly when pump disconnected from AC power; pump shuts down during operation or cannot sustain operation on battery alone
Ranked causes
- 1. Battery ribbon cable disconnected or loose (common)
- 2. Battery charging circuit failure (occasional)
- 3. Battery chemistry degraded or cell failure (occasional)
- 4. Battery calibration required (occasional)
Inspect and reseat battery ribbon cable
- Test point
- Battery ribbon cable connector on Interconnect PCB
- Expected
- Connector fully seated, no looseness
3 more checks with pass and fail actions, 4 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Learn Error - Remote Not in Teach Mode
Learning pump displays error message 'Learn Error - Remote Not in Teach mode' when attempting configuration cloning from Teacher pump. Communication fails during infrared data transfer.
Ranked causes
- 1. Teacher pump not in Teach Mode or infrared ports misaligned (common)
- 2. Teacher and Learning pumps have different software versions (occasional)
- 3. Learning pump not properly configured in Learn Mode (occasional)
- 4. Pump hardware malfunction or damaged Interconnect PCB (rare)
Verify Teacher pump in Teach Mode
- Test point
- Profile Settings menu
- Expected
- Teach Mode selected and active
2 more checks with pass and fail actions, 7 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Alarms do not sound or sound faintly patient safety
Speaker produces no sound or very low volume for alarms; audio may be inaudible in clinical environment
Ranked causes
- 1. Alarm volume configured to lowest level (common)
- 2. Speaker grid holes obstructed (occasional)
- 3. Speaker failure (rare)
Review alarm volume setting (V3 pumps)
- Test point
- Custom Program audio settings menu
- Expected
- Alarm volume set to medium or high level
3 more checks with pass and fail actions, 4 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
LCD has poor contrast or is unreadable
Display text is dim, hard to read, or has low contrast; visibility impaired regardless of ambient lighting
Ranked causes
- 1. LCD contrast setting at minimum or too low (common)
- 2. LCD negative supply voltage fault (rare)
- 3. LCD or Main PCB hardware failure (rare)
Run Adjust Contrast utility
- Test point
- Biomed > Calibration > Adjust Contrast menu
- Expected
- Contrast adjustment slider available and responsive; display improves with slider adjustment
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
No charge light illuminated
Battery charge indicator LED does not light when pump connected to AC power; may indicate battery not charging or power supply problem
Ranked causes
- 1. AC power not connected or pump not powered on (common)
- 2. Both AC and charge indicators off; indicator light or display issue (occasional)
- 3. Battery not charging or charger failure (occasional)
Verify AC power connection
- Test point
- AC power inlet on pump rear
- Expected
- AC cord plugged into power outlet; AC indicator LED lit
2 more checks with pass and fail actions, 3 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Occlusion alarms occur too frequently patient safety
Pump triggers occlusion alarm repeatedly during normal infusion; false alarms without actual line blockage
Ranked causes
- 1. Occlusion alarm limit set too low in Configuration (common)
- 2. High infusion line backpressure due to setup or medication (common)
- 3. Force sensor miscalibration or drift (occasional)
Review occlusion alarm limit setting
- Test point
- Pump Configuration occlusion limit value
- Expected
- Occlusion limit set to appropriate level for line setup and medication
2 more checks with pass and fail actions, 4 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Alarms do not sound audibly caution
Alarms either do not sound or sound very faintly
Ranked causes
- 1. Alarm volume configured to lowest level (common)
- 2. Speaker failure (occasional)
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery not working message
Pump displays battery failure message or no battery response
Ranked causes
- 1. Battery ribbon cable disconnected (common)
- 2. Battery pack failure (occasional)
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery not working message displayed
Pump displays 'Battery Problem: Battery not working' message; battery pack is not communicating with pump electronics
Ranked causes
- 1. Battery ribbon cable disconnected or loose (common)
- 2. Battery pack defective (common)
Inspect battery ribbon cable connection
- Test point
- Battery ribbon cable connector on Interconnect PCB (inside case bottom)
- Expected
- Connector fully seated and locked
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: AC line leakage (Medfusion 3500BC) high voltage
Verify enclosure and earth leakage current on 3500BC model with functional earth ground
Ranked causes
- 1. Enclosure leakage exceeds 100 micro-amps (rare)
- 2. Earth leakage exceeds 100 micro-amps through AC power cord earth conductor (rare)
Connect pump to Safety Analyzer
- Test point
- AC power inlet
- Expected
- Analyzer configured in Line Leakage mode
4 more checks with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Syringe size sensor
Load calibration slugs into barrel clamp and adjust position to find lowest size reading for both small and large standards, recording count values.
Ranked causes
- 1. Syringe size sensor requires calibration (common)
- 2. Large standard calibration needed (common)
Verify small standard size reading
- Test point
- Barrel clamp with small slug
- Expected
- Lowest size reading achieved when clamp perpendicular and adjusted back/forth
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
General inspection caution
Annual maintenance visual and physical inspection of pump components, power cord, labels, and housing
Ranked causes
- 1. Physical damage or wear on pump components (occasional)
- 2. Loose internal or external parts detected during inspection (occasional)
Inspect for physical damage to housing and keypads
- Test point
- Pump housing and keypad surfaces
- Expected
- No cracked housings or torn keypads
9 more checks with pass and fail actions, 9 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Indicator lights do not flash
Status indicator lights do not illuminate during startup or function
Ranked causes
- 1. Keypad connection loose (common)
- 2. Keypad failure (occasional)
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Indicator lights do not flash during startup or with alarms
LED indicator lights on pump do not illuminate during power-up or in response to alarms and function activation; display may be dark or unresponsive
Ranked causes
- 1. Keypad cable loose or disconnected from Main PCB (common)
- 2. Keypad or LED circuit failure (rare)
Inspect keypad cable connection to Main PCB
- Test point
- Keypad ribbon cable connector on Main PCB
- Expected
- Connector fully seated and locked; no movement or looseness
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Keypad key does not respond to presses
One or more keypad buttons do not register when pressed; no response or stuck key condition
Ranked causes
- 1. Keypad connection loose or disconnected (common)
- 2. Keypad hardware failure (rare)
Run Keypad Test in Biomed diagnostics
- Test point
- Biomed > Diagnostics > Keypad Test menu
- Expected
- All keys pass diagnostic test; no failed keys reported
2 more checks with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
LCD display poor contrast
Liquid Crystal Display text or graphics not clearly visible
Ranked causes
- 1. LCD contrast setting too low (common)
- 2. LCD negative supply or display failure (occasional)
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Maximum infusion rate not available or set too low patient safety
Pump maximum delivery rate setting is lower than desired; maximum rate option in menu unavailable or locked
Ranked causes
- 1. Maximum rate configured low in pump Configuration (common)
- 2. Individual profile has lower maximum rate than global setting (occasional)
Review global Max Delivery Rate setting
- Test point
- Profile Settings > View Settings > Max Delivery Rate
- Expected
- Max Delivery Rate set to desired value or higher
3 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
No charge light indicator
Charge indicator light does not illuminate when battery charging or AC powered
Ranked causes
- 1. AC power not connected (common)
- 2. Battery charging issue (occasional)
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
AC power indicator test high voltage
Verify AC power indicator LED lights when pump plugged into AC source and extinguishes when unplugged
Ranked causes
- 1. AC power indicator LED malfunction or power supply issue (rare)
Verify AC indicator LED lights when connected to AC power
- Test point
- AC indicator LED on pump
- Expected
- AC indicator LED is lit
1 more check with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Adjust LCD contrast voltage
LCD display contrast is too light or too dark. Factory default is 00BF but may vary by display manufacturer.
Ranked causes
- 1. LCD contrast voltage requires adjustment (occasional)
Set contrast voltage
- Test point
- CONTRAST VOLTAGE
- Expected
- 00BF (or adjusted value per lighting conditions)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Annual maintenance: General inspection caution
Visual and functional inspection of pump housing, mechanical components, power cord, labels, and rubber feet for damage, wear, or loose parts.
Ranked causes
- 1. Physical damage or normal wear (unknown)
Inspect for obvious physical damage
- Test point
- pump housing, keypads, flippers, clamps
- Expected
- no cracked housings, torn keypads, or visible damage
8 more checks with pass and fail actions, 10 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Annual maintenance: Power-up test caution
Functional verification of alarm sounds, LED indicators, battery capacity, self-tests, display legibility, and AC/battery switching upon power-on.
Ranked causes
- 1. Power supply or display malfunction (unknown)
Plug AC power cord and verify AC/battery indicators light
- Test point
- AC power receptacle, AC indicator LED, battery charge indicator LED
- Expected
- both AC and battery indicators are lit
7 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery calibration required
CPI (Capacity Inaccurate) counter exceeds threshold; pump requires recalibration cycle
Ranked causes
- 1. Shallow discharge cycles accumulated since last calibration (common)
Monitor CPI value in Biomed > Diagnostics > Monitor Battery Status
- Test point
- Biomed > Diagnostics > Monitor Battery Status
- Expected
- CPI <= 80 Hex
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Battery depleted, pump loses calibration patient safety
Battery Depleted alarm occurs; pump loses all calibration information; approximately 5 minutes of operation remain before full disconnect; audible alarm continues from super-capacitor
Ranked causes
- 1. Battery capacity below 1600 mA-hours (common)
Recharge pump and monitor battery status
- Test point
- Biomed > Diagnostics > Monitor Battery Status
- Expected
- After several minutes of recharging, gauge shows learned capacity; LMD value greater than 1600 mA-hours
2 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: AC input assembly replacement high voltage
Steps to remove and install AC input module assembly with verification of AC power indicator function.
Ranked causes
- 1. AC Input Module Assembly failure or replacement required (unknown)
Verify AC power indicator lights after replacement
- Test point
- AC power indicator light
- Expected
- AC power indicator lights on
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: AC line leakage (Standard Medfusion 3000) high voltage
Verify enclosure leakage current and optional CF-rated patient contact leakage are within specification
Ranked causes
- 1. Leakage current exceeds Class II BF limit of 100 micro-amps (rare)
Connect pump to Safety Analyzer
- Test point
- AC power inlet
- Expected
- Analyzer configured in Line Leakage mode
3 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: AC line leakage (standard) high voltage
Verify electrical leakage current within acceptable limits for patient safety (BF or CF rating compliance)
Ranked causes
- 1. AC leakage current out of specification (unknown)
Measure enclosure leakage current (BF rating)
- Test point
- Plunger driver tube or center post of DC input jack
- Expected
- Less than 100 micro-amps in normal setting, <100
- Tools
- Safety Analyzer in Line Leakage mode
1 more check with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: AC power supply replacement high voltage
Steps to remove and install AC power supply PCB with verification of AC power indicator light function.
Ranked causes
- 1. AC Power Supply PCB failure or replacement required (unknown)
Verify AC power indicator lights after replacement
- Test point
- AC power indicator light
- Expected
- AC power indicator lights on
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Adjust contrast (voltage)
Adjust LCD display contrast voltage setting using up/down keys. Factory default is 00BF; adjust higher or lower based on lighting conditions.
Ranked causes
- 1. Display contrast requires adjustment for lighting conditions (occasional)
Adjust contrast voltage setting
- Test point
- LCD display
- Expected
- Visual clarity appropriate for ambient lighting conditions
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: All sensors
Recalibration required after replacing case top to ensure proper sensor operation and pump accuracy.
Ranked causes
- 1. Case top replacement affects sensor alignment (common)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Battery charge and performance status
Monitor battery NiMH/NiCad cell capacity, charge level gauge accuracy, and shallow discharge cycle count to maintain performance
Ranked causes
- 1. Battery gauge accuracy degraded or capacity low (occasional)
Monitor battery LMD (Last Measured Discharge) capacity
- Test point
- Biomed > Diagnostics > Monitor Battery Status menu
- Expected
- LMD ≥ 1600 mA-hours, ≥1600
- Tools
- Pump Biomed diagnostics menu
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Battery full discharge-recharge cycle
Execute complete battery discharge to depleted alarm, then recharge to recalibrate gauge and relearn true battery capacity
Ranked causes
- 1. Battery calibration required (CPI threshold exceeded or new battery installed) (occasional)
Verify pump connected to AC and charge level reaches 99-100%
- Test point
- Biomed > Diagnostics > Monitor Battery Status gauge
- Expected
- Charge Level 99-100%
2 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Battery monitor accuracy
Battery gauge recalibration to ensure correct capacity reading and low battery alarm accuracy
Ranked causes
- 1. CPI (Capacity Inaccurate) exceeds threshold after shallow discharge cycles (common)
Connect pump to AC power
- Test point
- AC power inlet
- Expected
- Pump powered from AC mains
4 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Bottom housing replacement
Steps to remove and install bottom housing assembly with serial number label configuration based on installed Interconnect PCB model.
Ranked causes
- 1. Bottom housing damage or replacement required (unknown)
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Flow delivery accuracy
Verify syringe plunger travel distance matches expected range for infusion rate accuracy at 300 ml/hr with 50 ml volume limit
Ranked causes
- 1. Flow calibration out of specification (unknown)
Measure syringe plunger travel distance for flow accuracy
- Test point
- Syringe flange to plunger distance
- Expected
- B-D 60cc: 3.473" to 3.615"; B Braun Perfusor/Omnifix 50cc: 3.146" to 3.275"; Fresenius 50cc: 2.904" to 3.023"; Monoject 60cc: 3.473" to 3.615"; Terumo 60cc: 2.901" to 3.020" inches, ±0.071" (B-D), ±0.065" (B Braun), ±0.060" (Fresenius), ±0.07
- Tools
- Calipers, 50/60 cc Luer-lock syringe, Safety Analyzer
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Force sensor verification caution
Verify force sensor readings are within acceptable range using calibration kit with force gauge; check at no load, 5 pounds, and 15 pounds applied force.
Ranked causes
- 1. Force sensor calibration drift or error (unknown)
Verify force reading with no syringe loaded
- Test point
- screen force display
- Expected
- between –0.7 and +0.7 pounds, ±0.7 pounds
2 more checks with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Main PCB replacement
Steps to remove and install Main PCB with reconnection of all cable and sensor connections. Requires serial number and Configuration version for P.A.S.S. pumps.
Ranked causes
- 1. Main PCB failure or replacement required (unknown)
Reconnect all cable connections on Main PCB
- Test point
- J10, J3, J6, J12, J2, J4, J11 connectors
- Expected
- All cables connected and secured per procedure
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Plunger position sensor
Plunger position sensor drift or misalignment. Requires calibration of position sensor reference points.
Ranked causes
- 1. Plunger position sensor requires recalibration (common)
Verify plunger position sensor minimum and maximum values
- Test point
- PLUNGER POS DATA
- Expected
- 151 to 901 COUNTS, to 901 COUNTS
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Plunger position sensor verification
Annual maintenance check to verify plunger position sensor readings are within specification using small and large calibration slugs
Ranked causes
- 1. Plunger position sensor out of calibration (unknown)
Verify small calibration slug position reading with ~0.1 lbs force
- Test point
- Position reading on screen
- Expected
- between 0.680" and 0.720", inclusive inches, ±0.02
1 more check with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Position and size
Sensor recalibration needed after case handle replacement to maintain accurate syringe position and size detection.
Ranked causes
- 1. Case handle replacement affects position/size sensor calibration (common)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Pressure sensor
Pressure sensor calibration or offset adjustment after repair or drift detection.
Ranked causes
- 1. Pressure sensor requires recalibration (common)
Verify pressure sensor values
- Test point
- PRESSURE DATA
- Expected
- 0 COUNTS
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Save changes and exit
Save new calibration values and exit Biomed Calibration menu. Option to exit without saving if calibration error occurred.
Ranked causes
- 1. Need to save calibration changes after adjustment (common)
Confirm calibration changes ready to save
- Test point
- Calibration menu
- Expected
- All required calibrations completed
2 corrective actions and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Size and position sensor combined
Combined recalibration of both syringe size and plunger position sensors when both require adjustment.
Ranked causes
- 1. Size and position sensors require recalibration (common)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Small syringe size and position sensor check caution
Verify position sensor reading is within acceptable range when plunger driver is loaded on calibration slug with light force applied.
Ranked causes
- 1. Position sensor calibration drift or error (unknown)
Verify position sensor reading with calibration slug loaded
- Test point
- screen position display
- Expected
- between 0.660" and 0.740", inclusive inches, ±0.04 inches
- Tools
- Small calibration slug, calipers with 0.001" resolution
Calibration: Syringe size sensor verification
Annual maintenance check to verify syringe size sensor readings are within specification using small and large calibration slugs
Ranked causes
- 1. Syringe size sensor out of calibration (unknown)
Verify small calibration slug size reading
- Test point
- Size reading on screen
- Expected
- between 0.256" and 0.272", inclusive inches, ±0.008
1 more check with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: Tubing holder size
Recalibration of size sensor needed after tubing holder replacement to maintain accurate syringe size detection.
Ranked causes
- 1. Tubing holder replacement affects size sensor calibration (common)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Calibration: View calibration data
Display pump calibration data on screen for factory service or troubleshooting. Shows Force, Plunger Position, Pressure, and Syringe Size count values.
Ranked causes
- 1. Need to verify calibration data for troubleshooting (occasional)
Review Force calibration data
- Test point
- Calibration data screen
- Expected
- Force counts display (reference: 42-475 COUNTS range)
2 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Clutch or clutch cam replacement caution
Clutch halves or cam gear requires removal and reinstallation in carriage assembly during service.
Ranked causes
- 1. Worn or damaged clutch or cam requiring replacement (unknown)
Remove e-ring from cam in carriage plate
- Test point
- Cam in carriage plate
- Expected
- E-ring removed
- Tools
- Needle nose pliers or hemostats
3 more checks with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Flow delivery rate outside acceptable tolerance patient safety
Measured syringe plunger travel does not fall within specified range for selected syringe type
Ranked causes
- 1. Pump delivery mechanism calibration error (unknown)
Configure pump for flow delivery accuracy test
- Test point
- Begin Infusion screen
- Expected
- Rate of 300 ml/hr selected with volume limit of 50 ml
5 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Installation/Quick check-out: Force sensor verification with no load caution
Verify force reading is within nominal range when pump is powered on with no syringe loaded.
Ranked causes
- 1. Force sensor zero offset error (unknown)
Verify force reading with no syringe loaded
- Test point
- screen force display
- Expected
- between –0.7 and +0.7 pounds, ±0.7 pounds
Keyclick beep is faint or absent
Button click sounds from keypad are faint or not heard
Ranked causes
- 1. Keyclick audio configured to lowest level or disabled (common)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Keyclick beeps are faint or absent
Key press feedback sounds (beeps) are inaudible or very quiet; audio feedback disabled or configured to low level
Ranked causes
- 1. Keyclick volume configured to lowest level or disabled (common)
Check keyclick loudness setting (V3 pumps)
- Test point
- Custom Program audio settings menu
- Expected
- Keyclick loudness set to medium or high level; not at minimum
1 more check with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Keypad button does not respond
Pressing keypad button does not register or control pump function
Ranked causes
- 1. Keypad mechanical or connection failure (common)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Keypad replacement
Keypad requires removal from top housing and disconnection of interconnect and backlight cables; removal of ground tab.
Ranked causes
- 1. Damaged keypad or membrane switch requiring replacement (unknown)
Disconnect Interconnect ribbon cable from Main PCB
- Test point
- J9 connector on Main PCB
- Expected
- Interconnect cable unplugged
4 more checks with pass and fail actions, 1 corrective action, and part numbers are in ServiceForge. Connect ServiceForge to your AI
LCD and backlight assembly replacement
Old-style or new-style LCD display with backlight requires removal and reinstallation; backlight orientation critical for function.
Ranked causes
- 1. Damaged LCD display or backlight assembly requiring replacement (unknown)
Disconnect display cable from Main PCB
- Test point
- J12 connector on Main PCB
- Expected
- Display cable disconnected
4 more checks with pass and fail actions, 2 corrective actions, and part numbers are in ServiceForge. Connect ServiceForge to your AI
Libraries not available in configuration
Drug infusion libraries do not appear in pump configuration menu
Ranked causes
- 1. Libraries disabled or cleared in configuration (common)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Low battery capacity detected
LMD (Last Measured Discharge) below threshold; battery replacement needed
Ranked causes
- 1. Battery capacity degraded below 1600 mA-hours (common)
Monitor LMD value in Biomed > Diagnostics > Monitor Battery Status
- Test point
- Biomed > Diagnostics > Monitor Battery Status
- Expected
- LMD >= 1600 mA-hours
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
Maximum infusion rate not available
Maximum flow rate setting option does not appear or is limited
Ranked causes
- 1. Maximum rate configured too low (common)
1 corrective action and part numbers are in ServiceForge. Connect ServiceForge to your AI
More symptoms
- No drug libraries, profiles, or categories available
- Occlusion alarm does not occur during test
- Occlusion alarms occur frequently
- Plunger cable replacement
- Power-up test
- Pump activation before manual procedures
- Pump cleaning and disinfection
- Pump option or feature is not available
- Pump requires annual maintenance
- Syringe manufacturer not available
- Syringe manufacturer not available in pump Configuration
- System Fault alarm activated
- Watchdog Fail-Safe alarm triggered
- Watchdog or system failure alarm
14 more symptoms with ranked causes and checks are in ServiceForge. Connect ServiceForge to your AI
Error codes
| Code | Meaning | Trigger | Severity |
|---|---|---|---|
A2D Reference Voltage BGND Test | Analog-to-digital converter reference voltage invalid during background self-test | Background self-test measured invalid range on ADC reference voltage | critical |
A2D Reference Voltage BGND Test | Invalid range on ADC reference voltage | Background self-test execution | error |
ACU Power Strobe Failure | Auxiliary Control Unit processor not maintaining power strobe signal | Self-test found ACU processor not maintaining power strobe | critical |
ACU Watchdog Failure | Auxiliary Control Unit watchdog alarm signal active | Self-test found ACU watchdog alarm signal active, processor failed to pet watchdog | critical |
Analog Supply BGND Test | Analog power supply voltage outside valid range during background self-test | Background self-test measured invalid range on analog supply voltage | critical |
Aux Controller Unit Post | ACU processor failed motor current shutdown during watchdog alarm test | Power-up self-test found ACU processor failed to shut down motor current during watchdog test | critical |
Background CRC Test Timeout | Software timing failure in cyclic redundancy check during background test | Software timing failure during background CRC test | critical |
Background Self Test Timeout | Software timing failure in background self-test | Background self-test execution | error |
Background Self Test Timeout | Software timing failure during background self-test operation | Software timing failure during background self-test | critical |
Backup Audible Alarm Post | Backup audible alarm not working at correct power or frequency | Power-up self-test | warning |
Backup Critical Data Corrupted | Backup configuration data lost, primary data used to restore | Backup critical data in non-volatile EEPROM is lost | info |
Battery Communication Timeout | Battery gauge not communicating with pump | Battery current detected but gauge not responding | warning |
Battery Depleted alarm | Battery is completely discharged and pump cannot operate | Battery voltage drops to minimum usable level during unplugged operation | critical |
Battery Not Charging | Battery is not charging despite external power present | AC or DC external power detected but battery not charging | warning |
Battery Not Working | Battery very low while pump connected to external power | Very low battery signal detected during AC/DC power connection | warning |
Calculated Rate Out of Range | Pump calculated a rate that is not valid based on physical limits | Invalid combination of entered infusion parameters or syringe parameters | unknown |
Calibration Required | Sensor calibration data test failed | Power-up or calibration Save operation showed calibration data failure | error |
Calibration Required | Calibration values in non-volatile memory invalid or missing | Calibration values stored in EEPROM are invalid, typically after new main board installation | critical |
Check Clutch / Plunger Lever | Plunger driver motion is not correct | Position potentiometer senses plunger driver not moving correctly | unknown |
Check Syringe Barrel Clamp | Syringe barrel clamp sensor has difficulty verifying clamp position | Certain syringe models/sizes; barrel clamp lifted during power-up | unknown |
Check Syringe Flange Sensor | Syringe not loaded correctly as sensed by flange sensor | Syringe flange sensor detects improper loading or sensor failure | unknown |
Check Syringe Plunger Sensor | Syringe not loaded correctly as sensed by plunger sensor | Plunger sensor detects incorrect loading or Syringe Plunger Driver moved during startup | unknown |
Check Syringe Plunger Sensor | Pump detected plunger loaded when no syringe present | At power-up when barrel clamp sensor indicates no syringe | critical |
Clear TVD to Start Infusion | Total volume delivered exceeds programmed limit and must be cleared | TVD or TDD exceeds volume limit setting | info |
Completing System Initialization | User pressed start before background self-tests completed | User presses start button before pump self-testing completes at power-up | info |
Completing System Initialization | Self-tests still running when user attempted to start infusion | User presses Enter before background self-tests complete after power-up | info |
Control Key Switch BGND Test | Keypad key detected stuck on during continuous background self-test | Continuous background self-test found key stuck on | critical |
Control Key Switch Post | Keypad key detected stuck on during power-on self-test | Power-on self-test found key stuck on keypad | critical |
Control Key Switch Post | Single keypad key pressed for extended duration | Key pressed for longer than 7 seconds; or locked keypad key pressed longer than 1 minute | error |
Critical Data Block BGND Test | Critical delivery settings RAM corrupted as detected by background CRC test | Background self-test showed critical data block RAM corrupted via CRC test failure | critical |
Critical Data Block Post | Configuration data backup and primary CRC mismatch | Backup and primary configuration data fail CRC agreement | critical |
Critical Data Block Post | Primary and backup configuration data in EEPROM do not agree | Power-up self-test found primary and backup configuration/library data both good but not matching | critical |
Critical Data Failure | Settings reverse calculation verification failed or critical flags invalid | After programming settings, pump verification calculation failed or critical software flags invalid | critical |
Critical Data Failure | Settings validation or critical flag failure | After programming settings | error |
D2A Offset Voltage BGND Test | Force sensor offset signal failure in DAC | Background self-test found failure in force sensor offset signal | critical |
Data Does Not Match Previous Entry | User confirmation value does not match original entry | When confirmation of user-entered data is required but values don't match | info |
Default Configuration Restored | All configuration settings returned to factory defaults | Both primary and backup configuration lost in EEPROM | warning |
Depleted Battery | Battery fully discharged below low voltage threshold | Battery voltage measured by gauge falls below low voltage threshold | warning |
Depleted Battery (System Failure) | Battery voltage critically low, delivery stopped | Battery voltage measured by pump gauge is too low | critical |
Depleted Battery (System Failure) | Battery fully discharged below low voltage threshold | Battery voltage drops below fully depleted threshold | critical |
Display Controller Post | LCD display test failure detected during power-up self-test | Power-up self-test failure in LCD display controller | critical |
External COM Task Timeout | External device sending commands too quickly or too many invalid commands | External computer/device sending excessive/invalid commands to pump | error |
Flash Memory BGND Test | Program memory CRC failure detected during background self-test | CRC failure found in program memory during background self-tests | critical |
Flash Memory Post | Program memory CRC failure detected during power-up self-test | CRC failure found in program memory during power-up self-tests | critical |
Force Sensor BGND Test | Force sensor signal out-of-range or not responding to bridge test during background test | Background self-test found force sensor signal out-of-range or no response to bridge test signal | critical |
Force Sensor Bgnd Test | Force sensor self-test failed | Self-test performed on force sensor and failed; plunger driver moved or received hard bump during startup | unknown |
Force Sensor Bridge Test | Force sensor bridge shows no voltage change during test | Background self-test execution | error |
Force Sensor Bridge Test | Force sensor bridge strain gauge no voltage change when test signal asserted | Software sensed no voltage change when sensor test signal was asserted | critical |
Force Sensor Test | Force sensor output did not change when DAC offset voltage changed | Power-up self-test found force sensor output not responding to DAC offset change | critical |
History Data Corrupted | Infusion history log is corrupted | Software unable to retrieve history data in 6 consecutive attempts | info |
Improper Shutdown | Previous power-down did not occur through normal power key press | Pump powered on; last shutdown was not via power button (e.g., power loss, crash) | warning |
Improper Shutdown | Pump powered off without proper shutdown procedure | Power-down did not occur through pressing power button | info |
Infusion Complete | Programmed infusion volume delivered successfully | Infusion reached the set volume limit | warning |
Infusion Complete | Infusion has reached programmed volume limit | Delivered volume reaches set volume limit | info |
Input Out of Range - Greater Than Max Value | User-entered value exceeds maximum allowable limit | User attempts to enter number greater than maximum value allowed | info |
Input Out of Range - Less Than Min Value | User-entered value below minimum allowable limit | User attempts to enter number less than minimum value allowed | info |
Input Task Timeout | Software timing failure in input processing task | Software timing failure in input task | critical |
Internal A2D Failure | 10-bit analog-to-digital converter internal failure detected | Software self-test identified failure in 10-bit ADC | critical |
Invalid Infusion Parameter Combination | Parameter combination does not allow valid flow rate calculation | User entered invalid parameter combination or wrong syringe size for Drug Program | warning |
Invalid Interrupt | Software attempted to execute invalid interrupt vector | Software/hardware detected invalid interrupt execution | critical |
Invalid Interrupt & System Advisory: Improper Shutdown | Critical interrupt error coinciding with improper shutdown | Invalid interrupt detected along with improper shutdown event | critical |
Invalid Interrupt & System Advisory: Improper Shutdown | Improper shutdown alarm combined with invalid interrupt condition | Simultaneous improper shutdown and system interrupt detected | error |
Invalid Library Entry | Library entry was not defined correctly when created | Pump attempts to use improperly configured library entry | info |
Invalid Library Entry | Drug Program selected is invalid; pump cannot deliver it | Problem detected with selected Drug Program | error |
Invalid Rate for Syringe Size (V3 pumps only) | Programmed infusion rate incompatible with selected syringe type | When using E-plates library entries, changing syringe size causes mismatch | warning |
Invalid Syringe Size | Syringe size not recognized or improperly handled during delivery | Unrecognized syringe for model; barrel clamp lifted during delivery | unknown |
Invalid Syringe Size | Syringe size sensor reading does not match selected syringe manufacturer | Barrel clamp potentiometer sensor mismatch or barrel clamp lifted during delivery | critical |
KVO in Progress | Delivery switched to KVO (keep vein open) rate after volume limit reached | Infusion reached set volume limit and automatically changed to KVO rate | warning |
Learn Error - Remote Not in Teach Mode | Configuration cloning failed due to Teacher pump not ready or not communicating | Learning pump initiates learn process but cannot detect Teacher pump in active Teach Mode via infrared | error |
LED Task Timeout | Software timing failure in LED control task | Software timing failure in LED task | critical |
Limits Adjusted - Cannot Delivery All Doses | Soft limits adjusted to keep rate within allowable limits | PharmGuard soft limits and syringe parameters would result in rate outside allowable limits | warning |
Logic Supply Voltage BGND Test | Logic power supply voltage outside valid range during background self-test | Background self-test measured invalid range on logic supply voltage | critical |
Low Battery (1% drop incremental) | Battery capacity continues to drop below 10% | Each 1% drop in battery capacity after initial signal when power cord unplugged | warning |
Low Battery alarm | Battery charge level is low | Battery voltage drops below low threshold during unplugged operation | warning |
Low Battery (each 1% drop in capacity following initial sign | Battery capacity drops below 10%; percentage alerts continue if unplugged | Battery capacity measured at each percent below 10%; continues while on battery power | info |
Low Battery (initial signal) | Battery capacity fallen below 10% threshold | Initial low battery detection when capacity drops below 10% | warning |
Maintenance Is Recommended | Periodic maintenance reminder for annual maintenance testing | Maintenance interval has elapsed since last scheduled preventive maintenance | info |
MCU Power Strobe Failure | Main processor power strobe output signal test failure | Self-test of power strobe output port signal from main processor failed | critical |
Monitor Task Timeout | Software timing failure in monitoring task | Software timing failure in monitor task | critical |
Motor Failed to Stop Error | Stepper motor continues rotating after stop command issued | Software sensed motor rotation after stop pump motor command executed | critical |
Motor Not Running | Motor is not running | Erroneous sensor signal or mechanical/electrical failure | unknown |
Motor Not Running Error | Stepper motor does not rotate when rotation expected | Motor sensor did not detect stepper motor rotation | critical |
Motor Not Running Error | Motor sensor did not detect stepper motor rotation | Motor sensor failed to detect stepper motor rotation | critical |
Motor Rate Error | Stepper motor operating at incorrect speed | Stepper motor moving at wrong speed during operation | critical |
Motor Rate Error | Motor is not running at programmed rate | Motor speed not matching programmed rate | unknown |
Motor Rate Error | Motor rotation rate not matching expected value | Motor sensor did not measure correct stepper motor rotation rate | critical |
Motor Supply Voltage BGND Test | Motor power supply voltage outside valid range during background self-test | Background self-test measured invalid range on motor supply voltage | critical |
Motor Volume Limit Error | Motor has exceeded expected step count for programmed volume delivery | Motor runs more steps than required to deliver set volume limit | critical |
Neglected Pump (User Call-back) | Pump left in user input screen and inactive for extended time | Pump remains in user input screen (e.g., set rate, titrate rate) for more than 30 seconds | warning |
Non Critical Data Corrupted | Non-critical settings data in EEPROM lost or corrupted | Non-critical settings stored in EEPROM is lost | info |
Occlusion alarm | Line occlusion detected during infusion | Pressure rise in infusion tubing indicates blocked line | error |
Occlusion - Check Infusion Line | Infusion line is occluded | Force sensor in plunger driver senses occlusion when force exceeds set limit | unknown |
Occlusion - Check Infusion Line | High backpressure detected in infusion line due to blockage | Force sensor in plunger driver sensed occlusion when force exceeds set limit | critical |
Outside Range Limit - Silence Alarm to Continue | User-entered infusion rate outside established library safety limits | User enters rate which is outside of library limits | warning |
Periodic Callback - Silence Alarm to Continue | User-programmed periodic callback alarm activated | Periodic alarm set by user reaches scheduled time | warning |
PharmGuard Data Corrupted | PharmGuard Safety Data in EEPROM lost or unreadable | PharmGuard Safety Data stored in EEPROM is lost or corrupted | info |
PharmGuard Data Transfer is Recommended | PharmGuard Safety Data storage nearly full | PharmGuard Safety Data approaches storage capacity | warning |
Plunger Sensor Failure | Plunger position sensor voltage out of range | Software sensed plunger sensor voltage out of range | critical |
Positive Supply BGND Test | Power supply malfunction detected | Background self-test execution | error |
Positive Supply BGND Test | Positive power supply voltage out of valid range | Background self-test measured invalid positive supply voltage | critical |
Pressure Increasing - Check Infusion Line | Backpressure in infusion line is gradually increasing | Force sensor detects increasing pressure during infusion | warning |
Primary Audible Alarm BGND Test | No current detected in primary speaker | Background self-test execution | error |
Primary Audible Alarm Post | No current detected in primary speaker during power-up test | Power-up self-test | error |
Primary Critical Data Corrupted | Primary configuration data lost, backup data used to restore | Primary critical configuration data in EEPROM is lost | info |
Profile Does Not Match Last Settings Profile | Current pump profile does not match profile used for recalled settings | Recall Last Settings feature invoked for different profile than settings were programmed under | info |
Profile Does Not Match Last Settings Profile | Recall Last Settings incompatible with current delivery profile | User attempts Recall Last Settings but currently selected profile differs from saved profile | info |
Pump is Locked | Pump settings locked during active delivery | Pump in delivery mode with settings locked | info |
Pump Motor Drive Off Post | No current detected in stepper motor at power-up | Power-up self-test sensed no current in stepper motor | critical |
Pump Motor Drive Phase A Post | Stepper motor winding A open at power-up | Power-up self-test found stepper motor phase A winding open | critical |
Pump Motor Drive Phase B Post | Stepper motor winding B open at power-up | Power-up self-test found stepper motor phase B winding open | critical |
RAM BGND Test | RAM failure on Main PCB | Software test showed failure of RAM on Main PCB | critical |
Rate Below Recommended Min for Syringe Size | Programmed infusion rate below minimum recommended for syringe type | User programs rate lower than manufacturer recommendation for selected syringe | info |
Restricted Flow - Bolus Cancelled | Bolus dose delivery cancelled due to flow restrictions | During bolus rate reduction, rate fell below main infusion rate or time extended past 59 minutes maximum | warning |
Restricted Flow - Bolus Cancelled | Bolus rate reduction resulted in rate below main rate or max time exceeded; bolus cancelled | During bolus dose rate reduction, calculated rate fell below main infusion rate or total time exceeded 59 minutes | warning |
Restricted Flow - Loading Cancelled | Loading dose rate reduction resulted in rate below main rate or max time exceeded; loading dose cancelled | During loading dose rate reduction, calculated rate fell below main rate or total time exceeded 59 minutes | warning |
Restricted Flow - Loading Cancelled | Loading dose delivery cancelled due to flow restrictions | During loading dose rate reduction, rate fell below main infusion rate or time extended past 59 minutes | warning |
Restricted Flow - Rate Reduced | Pump reduced infusion rate to overcome high backpressure during bolus or loading dose | High backpressure detected during bolus or loading dose delivery on Medfusion 3500 | warning |
Serial EEPROM Timeout | Serial EEPROM communication timeout on main board | Software test execution | error |
Set Time and Date | Real-time clock reset to default | Real-time clock reset when battery depleted or main board supply discharged | warning |
Set Volume Limit Before KVO | Volume limit must be set before KVO rate can be programmed | User attempts to set KVO rate without first setting volume limit | warning |
SPI BUS Timeout | SPI bus component failure timeout | Software test execution | error |
Supercap Post | Super-capacitor insufficient charge at power-up | Power-up self-test sensed insufficient charge in super-capacitor | warning |
Syringe Does Not Match Library Entry | Loaded syringe size does not match library entry specification | When using E-plates library entries, loaded syringe does not match stored syringe size | info |
Syringe Empty | Plunger driven to end of syringe barrel, no fluid remains | Plunger driver position potentiometer senses syringe empty position | critical |
Syringe Empty | Syringe has been completely emptied | Plunger driver position potentiometer reaches empty position for loaded syringe size | error |
Syringe Empty - Manual | Syringe reached empty position; user can resume to deliver residual fluid until occlusion limit reached | After Syringe Empty alert, user presses resume to extract remaining fluid in syringe barrel | error |
Syringe Empty - Manual | After reaching empty position, manual continuation option available | After Syringe Empty alarm, user presses Enter to resume | critical |
Syringe Flange Not in Place | Syringe flange is not properly inserted | Syringe not loaded correctly or flange sensor failure | unknown |
Syringe Flange Not in Place | Plunger flange not detected in pump when syringe loaded | When syringe is loaded but pump does not detect flange via barrel clamp sensor | critical |
Syringe Flange Sensor Failure | Syringe flange sensor voltage out of range | Software sensed syringe sensor voltage out of range | critical |
Syringe Near Empty | Syringe has only a few minutes of fluid remaining | Plunger position indicates low fluid volume | warning |
Syringe Plunger Not in Place | Pump does not detect plunger in barrel when syringe loaded | When syringe is loaded but pump does not detect plunger via barrel clamp sensor | critical |
Syringe Plunger Not in Place | Syringe plunger is not properly positioned | Syringe not loaded correctly as sensed by barrel clamp size sensor or plunger sensor failure | unknown |
SYSTEM ADVISORY – BATTERY NOT WORKING | Battery malfunction or disconnection detected | Battery gauge detects failure or absence of battery power | warning |
System Advisory - Description | Generic system advisory alert with additional description | Various system-level advisory conditions | info |
System Failure - Description | Generic system failure alert with additional description | Various critical system failure conditions | critical |
Time Base BGND Test | System time base does not agree with time of day clock | Background self-test found MCU time base did not match clock tick | error |
Time of Day Clock Post | System time base does not agree with time of day clock at power-up | Power-up self-test found MCU time base did not match clock tick | error |
Time of Day Clock Timeout | Time of day clock failed to communicate | Time of day clock failed to communicate during software test | error |
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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.