FDA Device Intelligence
Home › HCMED INNOVATIONS CO., LTD. › Aerogen® Go

Aerogen® Go

HCMED INNOVATIONS CO., LTD. · Model 04EE12000012 · UDI-DI 04719873130214

CAF Prescription
1
510(k) clearances
3,267
Adverse events (43 deaths)
36
Recalls
191
Facilities

Description

The Aerogen Go Vibrating Mesh Nebulizer is designed for a single patient, multiple uses, and mainly composed of a Main Unit and a Medication Reservoir. The Main Unit contains the control circuitry and the firmware to control the vibrating mesh module in the Medication Reservoir and is powered by 2 AA alkaline batteries or an AC adaptor. This AC adaptor is in the sales package.

Recalls

DateFirmReason
2023-08-04MEDLINE INDUSTRIES, LP - NorthfieldProduct dispositioned for scrap for sterility failure investigation that was inadvertently shipped to customers.
2021-03-31Smiths Medical ASD Inc.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.
2018-08-29SANRAI INTERNATIONAL LLCThe product was designed for 120V usage and is being used in South Africa with 220V. There is a potential for the device to overheat and the mouthpiece can pop off.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.