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Device Lab 58

Nebulizer

Nebulizer in the BMEssentia 3D Device Lab

A bench compressor drives air through small-bore tubing into the base of a separate transparent cup with a conical lower body. The gas leaves a jet orifice at close to the speed of sound, the pressure drop beside it draws liquid up a feed channel (the venturi), the liquid is sheared into a spray, and the spray is thrown at an internal baffle that captures every large droplet and drains it back. What leaves through the cup top to the mouthpiece or mask is what the baffle let past.

Also called: Nebuliser. Arabic: جهاز الرذاذ. Device Lab 58 of 69 in BMEssentia Medical City, 2 configurations.

Overview: the configurations

Pneumatic jet cup driven by a bench compressor

A bench compressor drives air through small-bore tubing into the base of a separate transparent cup with a conical lower body. The gas leaves a jet orifice at close to the speed of sound, the pressure drop beside it draws liquid up a feed channel (the venturi), the liquid is sheared into a spray, and the spray is thrown at an internal baffle that captures every large droplet and drains it back. What leaves through the cup top to the mouthpiece or mask is what the baffle let past.

Self-contained vibrating-mesh unit

A palm-sized handheld unit carrying its mask on a short elbow, with a small liquid reservoir closed by a hinged lid. A piezoelectric ring vibrates a perforated plate at about a hundred kilohertz and each of about a thousand micrometre-scale apertures ejects droplets on its own. There is no compressor, no tubing and no gas flow anywhere in it; two cells and an oscillator are the whole energy source.

How it works: the main parts

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

Enclosure and stand
The enclosure holds the energy source and keeps it upright and away from the liquid. On the jet configuration it is a moulded clamshell box standing on a table or the floor, with a recess that stores the cup, mask and tubing; on the mesh configuration it is the palm-sized body of the handset itself.
Power switch and indicator
The power switch starts the energy source and its lit indicator says the source is running. On the jet unit it is a mains rocker switch with a lamp in it; on the handset it is a push button with a small light, drawing on the cells.
Compressor intake filter
A small felt or fibre pad behind a grille on the side of the compressor box, through which every litre of air the pump compresses is drawn. It keeps room dust out of the piston and, ultimately, out of the air that atomises the medicine.
Piston compressor and motor
A small electric motor driving a piston in a cylinder, with reed valves that let air in on the down-stroke and push it out on the up-stroke. It sits on soft mounts inside the box and is the whole energy source of the jet configuration: it supplies both the energy that shatters the liquid and the gas that carries the droplets away.
Small-bore air tubing
Two metres of clear plastic tube, 4 mm in bore, carrying compressed air from the compressor spigot to the connector under the cup. It is usually ignored, coiled in the storage recess, and it is the part most often stood on, rolled over or trapped under a bed wheel.
Jet orifice
6 mm across at the top of a nozzle moulded into the base of the cup. Compressed air from the tubing arrives below it and leaves through it as a fine, very fast jet.
Medication reservoir and cup body
The reservoir holds the liquid medicine, usually a few millilitres, while it is turned into aerosol. On the jet configuration it is the transparent cup with a conical lower body; on the mesh unit it is a small well sitting on the back of the vibrating plate.
Fill opening and graduations
The opening the liquid is poured or squeezed into, with graduation marks in millilitres on the clear wall. On the jet cup it is the open top of the cup body under its screw-on top; on the mesh unit it is the mouth of the small reservoir under its hinged lid.

Explore it in the Device Lab

Common faults and what to check

Most reported device problems (FDA MAUDE)

Device problemReports
Failure to Deliver420
Leak/Splash222
Connection Problem176
Infusion or Flow Problem174
Break170
No Flow132

Raw counts of adverse event reports for this device type (FDA product code CAF), 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.

Planned maintenance checks

From the BMEssentia procedure library: every 12 months, about 15 minutes, electrical class II, applied part type BF.

CheckPass when
Unit, filter and tubing
Inspect the inlet filter, tubing connector and case.
Filter clean.
Output
Measure compressor output or check the mesh aerosol output.
Per manufacturer.

Test instruments: Pressure gauge or flow meter (compressor).

Recent FDA recalls

RecallProduct and reason
Z-2514-2023
2023-09-14
MEDLINE INDUSTRIES, LP - Northfield: HUDSON RCI Addipak, UNIT DOSE VIALS, 5mL Sterile 0.9% NaCl Solution for Inhalation USP. REF RHUD59U
Product dispositioned for scrap for sterility failure investigation that was inadvertently shipped to customers. Root cause: Process control.
Z-1516-2021
2021-03-31
Smiths Medical ASD Inc.: ACE MDI Spacer with Small Mask - Product Usage: designed to assist with the delivery of aerosolized medications from
The firm became aware via complaints that one lot of ACE MDI Spacers with Small Masks and one lot of Palm Cups (Large) may have incorrect shipping box labels. Root cause: Process control.
Z-0710-2019
2019-02-04
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company: Portex 350 ml Sterile Water Humidifier w/5psi Adapt.
Lack of sterility assurance: leaking containers which could lead to exposure to infectious agents. Root cause: Process control.
Z-0711-2019
2019-02-04
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.
Lack of sterility assurance: leaking containers which could lead to exposure to infectious agents. Root cause: Process control.
Z-0712-2019
2019-02-04
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company: Portex 1000 ml Sterile Water USP Pour Bottle
Lack of sterility assurance: leaking containers which could lead to exposure to infectious agents. Root cause: Process control.

From the FDA recall database (openFDA), newest first, imported 2026-10-22. 36 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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