HUDSON RCI IPN927526Recalls & reported problems
Teleflex Incorporated · CONCHA NEPTUNE · Class 2
All models of HUDSON RCI (152)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704728500), received between Jun 14, 2024 and Jun 14, 2024 — classified as 1 malfunction.
3 other recalls cover devices cleared under the same FDA submission (K131912); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 14, 2024
RESPIRATORY THERAPIST (RT) RESPONDED TO VENT ALARMING. RT AND THE NURSE ASSESSED PATIENT AND EQUIPMENT. CLINICAL STAFF FOUND THE VENT CIRCUIT MELTED AND FUSED TOGETHER AND CREATED A 100% LEAK. AFTER RECOGNIZING THE ISSUE, CALLED A CHARGE RT AND CHANGED THE VENT AND THE CIRCUIT. ISSUE WAS SOLVED. HEATER HUMIDIFIER INVOLVED IN INCIDENT WAS A TRIAL NEPTUNE HEATER HUMIDIFIER AND CIRCUIT. AFTER INCIDENT, PATIENT WAS SWITCHED TO HOSPITAL-OWNED FISHER & PAYKEL HEATER HUMIDIFIER. BIOMEDICAL ENGINEERING INSPECTED THE EQUIPMENT. THE HEATER HUMIDIFIER APPEARS TO HAVE OVERHEATED THE INTERNAL WIRE OF BREATHING CIRCUIT. THIS CAUSED THE TUBING TO FUSE TOGETHER. VENTILATOR WAS ALSO INSPECTED, NO ISSUES FOUND.
Patient problems: Insufficient Information
MAUDE report 19536582 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K131912. One submission often covers many models, so check the product and lot details in each record.
- Z-1115-2020 · Dec 13, 2019 · TerminatedHUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port, REF 2414, humidifier nebulizer kit
- Z-1114-2020 · Dec 13, 2019 · TerminatedHUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kit
- Z-1558-2015 · Apr 1, 2015 · TerminatedTeleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only.
Other HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE) devices
- Fisher & Paykel Healthcare PT101USFisher & Paykel Healthcare Limited · Humidifier, Respiratory Gas, (Direct Patient Interface)2 recalls5 deaths1,068 reports
- HUDSON RCI IPN913776Teleflex Incorporated · HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE)436 reports
- F&P Optiflow+ OPT944Fisher & Paykel Healthcare Limited · Humidifier, Respiratory Gas, (Direct Patient Interface)5 deaths392 reports
- Fisher & Paykel Healthcare PT100USFisher & Paykel Healthcare Limited · Humidifier, Respiratory Gas, (Direct Patient Interface)2 recalls59 reports
- MR850 MR850JHUFisher & Paykel Healthcare Limited · Humidifier, Respiratory Gas, (Direct Patient Interface)93 reports
- HUDSON RCI HUD42500Medline Industries, Inc. · HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE)87 reports
- F&P Optiflow Junior 2 OJR412Fisher & Paykel Healthcare Limited · Humidifier, Respiratory Gas, (Direct Patient Interface)80 reports
- F&P Airvo 900PT561Fisher & Paykel Healthcare Limited · Humidifier, Respiratory Gas, (Direct Patient Interface)1 death56 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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