Puritan Bennett 560
Puritan Bennett · Model 560
• The internal lithium ion battery provides up to 11 hours of ventilator operation (depending on settings and other factors).* • A real-time battery life indicator shows how much battery time is left, in hours and minutes, based on settings. • The Puritan Bennett™ 560 ventilator is compact, lightweight (4.5 kg) and quiet (<30 dBA at 1 m). It transitions easily from hospital to home use. • Data portability is enabled via a USB memory device. The USB memory device makes it easy to transfer patient data from a home ventilator to a clinicians computer. • Ventilator parameters and alarm settings are linked to reduce the risk of clinically inappropriate settings. • Oxygen enrichment is available using a low pressure oxygen source. Utilize a measurement kit to monitor FiO2 levels
Key tips
- ·Never disable a low-pressure/circuit-disconnect alarm while troubleshooting - silence it, don't disable it.
- ·Verify the O2 supply source and pressure before assuming an internal fault.
- ·Circuit type must match the patient population (adult/pediatric/neonatal) - a mismatched circuit invalidates delivered volumes.
Typical Failure Modes
Failure patterns typical of this equipment class - general BMET reference, not verified against this exact unit's own service history unless flagged. Severity is a category-level estimate.
Exhalation valve leak / failure
HighSymptoms: Low exhaled tidal volume, high leak alarm, inability to maintain PEEP.
Root cause: Diaphragm/valve degraded by secretions and cleaning cycles.
Flow / pressure sensor drift
MediumSymptoms: Inaccurate delivered volume, false volume/pressure alarms.
Root cause: Sensor contamination or aging of differential-pressure transducer.
Compressor / turbine failure
HighSymptoms: Unable to reach set pressure, low-flow alarm, loud noise.
Root cause: Worn bearings or failed blower motor.
O2 blender / mixer fault
MediumSymptoms: FiO2 out of range, oxygen alarm.
Root cause: Failed solenoid or proportional valve in blender.
Serviceable Parts & Consumables
The parts a BMET typically services on this class of equipment. Service class and relative cost are general engineering estimates for the category, not figures from this unit's documentation. Part numbers appear only when pulled from this unit's own service manual. Always confirm intervals and pricing against the manufacturer.
Bacterial / HEPA filter
Consumable, replace per PM schedule.
Class ConsumableRel. cost $R&R Easy
Compressor / turbine module
Class Periodic replacementRel. cost $$$R&R Difficult
Rechargeable battery pack
Class Periodic replacementRel. cost $$R&R Fairly easy
O2 sensor (galvanic/paramagnetic)
Class Frequent wear itemRel. cost $$R&R Fairly easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Bacterial / HEPA filter Consumable, replace per PM schedule. | Consumable | $ | Easy |
| Compressor / turbine module | Periodic replacement | $$$ | Difficult |
| Rechargeable battery pack | Periodic replacement | $$ | Fairly easy |
| O2 sensor (galvanic/paramagnetic) | Frequent wear item | $$ | Fairly easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
PM Checklist
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
- ·Daily pre-use check: self-test, circuit integrity, alarm function
- ·Scheduled circuit and inspiratory filter replacement per manufacturer interval
- ·Flow and pressure sensor calibration verification
- ·Battery load test and runtime check
- ·Annual full PM and electrical safety test
Troubleshooting Approach
A structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Symptom: Exhalation valve leak / failure
- Confirm the presentation - typically low exhaled tidal volume, high leak alarm, inability to maintain PEEP - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: diaphragm/valve degraded by secretions and cleaning cycles.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the exhalation valve assembly per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Symptom: Flow / pressure sensor drift
- Confirm the presentation - typically inaccurate delivered volume, false volume/pressure alarms - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: sensor contamination or aging of differential-pressure transducer.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the flow / differential pressure sensor per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- ICU / CCU
- Emergency Department
- Operating Room (anesthesia-adjacent)
- NICU
- Respiratory Therapy department
- Patient transport
Documents & Manuals
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
Directions for Use-Puritan Bennett has determined that a service interval should be defined for the device. The firm has also determined that an exhalation filter should be employed when the device is in use.
- RECALL
Manufacturing defect at contract manufacturer, employee error, poor training, improper inspection.
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