Humidifier, Respiratory Gas, (direct Patient Interface)
Anesthesiology · 21 CFR 868.5450
Recent MDR events
18,072 adverse event reports on file
- Fisher & Paykel HealthcareJul 31, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02361
- Fisher & Paykel HealthcareJul 31, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02353
- Fisher & Paykel HealthcareJul 31, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02354
- Fisher & Paykel HealthcareJul 30, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02348
- Fisher & Paykel HealthcareJul 30, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02349
- Fisher & Paykel HealthcareJul 30, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02350
- Fisher & Paykel HealthcareJul 30, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02351
- Fisher & Paykel HealthcareJul 30, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02356
- Fisher & Paykel HealthcareJul 30, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02357
- Fisher & Paykel HealthcareJul 30, 2026MalfunctionFisher & Paykel Healthcare Ltd9611451-2026-02358
Event type breakdown
Recalls
69 recall events for this product code
- Fisher & Paykel Healthcare, Ltd.Open, ClassifiedOct 15, 2025
Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used with Disinfection Kit User Manual, REF: UI-185043723
When unintentionally disconnected from power source, humidifier device (used to deliver high flow warmed and humidified respiratory gases) may sound audible alert for less than 120 seconds, which may delay user awareness to reconnect power, which could lead to oxygen desaturation, hypoxia. Disinfection kit user manual updated to include checking the audible alert prior to use on a new patient.
Z-0158-2026 · View FDA record ↗ - Fisher & Paykel Healthcare, Ltd.Open, ClassifiedMay 15, 2024
Airvo 2 Humidifier, REF: PT101US, and myAirvo 2 Humidifier, REF: PT100US
Humidifier devices, used to deliver high flow respiratory therapy to patients, manufactured before 14 August 2017, have a speaker configuration that may result in distorted, intermittent or inaudible alarm sound levels. In the absence of an audible alarm, if there is an interruption to therapy, a patient may experience oxygen desaturation.
Z-1823-2024 · View FDA record ↗ - VapothermOpen, ClassifiedMar 17, 2023
Low Flow Disposable Patient Circuit for the Precision Flow System, Product Code PF-DPC-LOW
There have been reports of excessive condensation associated with certain lots of the Low Flow Disposable Patient Circuits (DPCs) used with Precision Flow System which may lead to excessive rainout.
Z-1272-2023 · View FDA record ↗ - TELEFLEX MEDICAL INCTerminatedFeb 7, 2020
HUDSON RCI COMFORT FLO Corrugated Humidification System, REF 2415, humidifier nebulizer kit
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column during high flow oxygen therapy.
Z-1112-2020 · View FDA record ↗ - TELEFLEX MEDICAL INCTerminatedFeb 7, 2020
HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote Temperature Port, REF 2416, humidifier nebulizer kit
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column during high flow oxygen therapy.
Z-1113-2020 · View FDA record ↗ - TELEFLEX MEDICAL INCTerminatedFeb 7, 2020
HUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kit
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column during high flow oxygen therapy.
Z-1114-2020 · View FDA record ↗ - TELEFLEX MEDICAL INCTerminatedFeb 7, 2020
HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port, REF 2414, humidifier nebulizer kit
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column during high flow oxygen therapy.
Z-1115-2020 · View FDA record ↗ - Vyaire MedicalTerminatedJan 24, 2018
Infant AirLife single-limb, continuous-flow circuit (Model AH132) containing AirLife Humidification Chamber, Model Number AH290.
Manufacturing error in humidification chamber may cause an overfill/overflow condition of the chamber. The may case a water back-up into the patient circuit resulting in an excessive amount of water entering the airway/lungs of the ventilated patient.
Z-0343-2018 · View FDA record ↗ - Vyaire MedicalTerminatedJan 24, 2018
Infant AirLife Dual-,limb, dual-heat, high-flow circuit (Model AH265) with AirLife Humidification Chamber, Model Number AH290.
Manufacturing error in humidification chamber may cause an overfill/overflow condition of the chamber. The may case a water back-up into the patient circuit resulting in an excessive amount of water entering the airway/lungs of the ventilated patient.
Z-0344-2018 · View FDA record ↗ - Vyaire MedicalTerminatedJan 24, 2018
Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification Chamber, Model Number AH290.
Manufacturing error in humidification chamber may cause an overfill/overflow condition of the chamber. The may case a water back-up into the patient circuit resulting in an excessive amount of water entering the airway/lungs of the ventilated patient.
Z-0345-2018 · View FDA record ↗
Registered firms
340 firms currently registered for this product code
Sunmed Group Holdings, Llc
Grand Rapids, MI, US
Sunmed Ap, Ltd., Warehouse No. 2
ZHUHAI Guangdong, CN
Galemed (xiamen) Co., Ltd.
XIAMEN Fujian, CN
Fisher & Paykel Healthcare, Inc.
IRVINE, CA, US
Breas Medical, Inc.
N Billerica, MA, US
Flexicare Medical Ltd.
RHONDDA CYNON TAFF Wales, GB
Productos Urologos De Mexico S.a. De C.v.
MEXICALI Baja California, MX
Rci Hudson De Mexico S. De Rl. De Cv.
Nuevo Laredo Tamaulipas, MX
Beijing Aeonmed Co., Ltd.
Sanhe Hebei, CN
Jianerkang Medical Co., Ltd.
Changzhou City Jiangsu, CN
Salter Labs
El Paso, TX, US
Medline Industries, Lp - Northfield
Northfield, IL, US
Cbr Enterprise Limited
Hong Kong, HK
Fisher & Paykel Healthcare S.a.de C.v.
Tijuana Baja California, MX
Uab Intersurgical
Visaginas Salcininkai, LT
Sterigenics Us Llc
Gurnee, IL, US
Laboratorios Biogalenic, S.a. De C.v.
Soyapango San Salvador, SV
Flight Medical Innovations Ltd.
PETACH TIKVA Central, IL
510(k) clearances
221 clearances for this product code
- Vapotherm, Inc.Apr 13, 2026
K254078 · HVT 2.0
- Flexicare Medical Limited.Jan 16, 2026
K251448 · FL-10000U Respiratory Humidifier
- Laboratorios Biogalenic S.A. DE C.V.Jan 14, 2026
K251419 · Laboratorios Biogalenic Sterile Water for Inhalation, USP
- Fisher & Paykel Healthcare, Ltd.Dec 19, 2025
K253479 · Optiflow Switch+ Filtered Nasal Interface with CO2 Sampling (AA042J)
- Medline Industries, LPJul 2, 2025
K250312 · Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus and Soft Plus Cannula Extra Small
- Fisher & Paykel Healthcare, Ltd.Jun 25, 2025
K251611 · Optiflow+ Nasal Cannula - Small (OPT942); Optiflow+ Nasal Cannula - Medium (OPT944); Optiflow+ Nasal Cannula - Large (OPT946); Optiflow+ Nasal Cannula Small (MYOPT9SMALL); Optiflow+ Nasal Cannula Medium (MYOPT9MEDIUM); Optiflow+ Nasal Cannula Large (MYOPT9LARGE)
- Laboratorios Biogalenic S.A. DE C.V.Jan 30, 2025
K242717 · Laboratorios Biogalenic Sterile Water for Inhalation, USP
- Medline Industries, LPDec 19, 2024
K241778 · Hudson RCI Comfort Flo® CubCannula