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Device Lab 10

Ventilator

Ventilator in the BMEssentia 3D Device Lab

A trolley-mounted turbine supplies air, an oxygen inlet supplies enrichment, and a heated chamber conditions the inspiratory gas. A dual-limb circuit returns exhaled gas through the expiratory valve.

Also called: Mechanical Ventilator, Breathing Machine. Arabic: جهاز التنفس الاصطناعي. Device Lab 10 of 69 in BMEssentia Medical City, 2 configurations.

Overview: the configurations

ICU turbine ventilator

A trolley-mounted turbine supplies air, an oxygen inlet supplies enrichment, and a heated chamber conditions the inspiratory gas. A dual-limb circuit returns exhaled gas through the expiratory valve.

Transport turbine ventilator

A compact turbine ventilator is secured beside a stretcher. A regulated cylinder supplies oxygen, a battery supplies electricity, and a passive heat and moisture exchanger conditions gas at the patient connection.

How it works: the main parts

What each part does, from the Ventilator lessons in the 3D Device Lab.

Ventilator body
The ventilator is a controlled gas-delivery and measurement system. Its case brings together a gas source, valves, sensors, electronics and protective functions.
Display and controls
The display is the operator’s window into set targets, measured values, breath timing and alarms. A target is an instruction; a measured value is evidence.
Air turbine and intake filter
The turbine draws room air through an inlet filter and generates the flow needed by the ventilator. It makes this representative architecture independent of a compressed medical-air outlet.
Oxygen inlet and regulated supply
The oxygen inlet connects the ventilator to an appropriate gas source. In the ICU scene a hose reaches a wall outlet; in transport a regulator connects a secured cylinder.
Gas mixing and inspiratory control
The mixing and delivery assembly brings together room air and oxygen, then controls the gas sent into the inspiratory limb. It is where a requested breath becomes an actuation task.
Inspiratory limb
The inspiratory limb carries conditioned gas from the ventilator toward the patient. Its corrugated wall allows movement, but flexibility does not make it immune to kinking, compression or disconnection.
Expiratory limb
The expiratory limb returns exhaled gas from the Y-piece to the ventilator’s expiratory assembly. Expiration is an active part of the control problem even when the patient’s recoil provides the driving pressure.
Expiratory valve
The expiratory valve controls the outlet through which exhaled gas leaves the circuit. It helps establish positive end-expiratory pressure, called PEEP.

Explore it in the Device Lab

Common faults and what to check

Guided fault cases in the Device Lab

Training cases written by BMEssentia for teaching.

Most reported device problems (FDA MAUDE)

Device problemReports
Device Displays Incorrect Message20,281
Mechanical Problem16,023
Output Problem12,955
Device Operates Differently Than Expected11,870
No Display/Image11,220
Battery Problem10,664

Raw counts of adverse event reports for this device type (FDA product code CBK, ONZ, NOU), all years. Not adjusted for the number of units in use, so they show what gets reported, not failure rates. Report text is never copied.

Recent FDA recalls

RecallProduct and reason
Z-2963-2026
2026-08-14
Maquet Critical Care AB: GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662
Maquet Critical Care AB, a subsidiary of Getinge, is voluntarily recalling Y sensor module, part of the SERVO-U/-N ventilator system, due to missing production safety electrical testing. Root cause: Under Investigation by firm.
Z-2735-2026
2026-07-28
ResMed Ltd.: Resmed Astral 100/150
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy. Root cause: Component design/selection.
Z-2525-2026
2026-06-23
Ventec Life Systems, Inc.: VOCSN+Pro package, REF: PRT-00853-000
Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of. Root cause: Vendor change control.
Z-1942-2026
2026-05-01
Ventec Life Systems, Inc.: VOCSN V+Pro package, REF: PRT-01198-000
Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could. Root cause: Process change control.
Z-1646-2026
2026-04-02
Philips Respironics, Inc.: Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths. Root cause: Software design.

From the FDA recall database (openFDA), newest first, imported 2026-10-22. 339 recalls on record for this device type. Recall text is the FDA's public text; each recall links to the official record.

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