HUDSON RCI IPN042780Recalls & reported problems
Teleflex Incorporated · HUMID VENT 2S FLEX DC STERILE · Class 1
All models of HUDSON RCI (152)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04026704347919), received between Oct 18, 2021 and Sep 15, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Apr 11, 2022Class IIOpen, Classified
Reports received of torn corrugated breathing tubes.
Z-1126-2022 · Root cause: Device Design · Recall details · FDA record ↗
Most reported problems
Device problems
- Break1
- Fluid/Blood Leak1
- Fracture1
- Gas/Air Leak1
- Material Rupture1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2025Fluid/Blood Leak; Material Rupture; Fluid/Blood Leak; Material Rupture
IT WAS REPORTED THAT: "ON (B)(6) 2025, THE ANESTHESIA MACHINE'S VENTILATION ALARM OCCURRED DURING THE OPERATION. THE PATIENT WAS UNABLE TO UNDERGO MECHANICAL VENTILATION. AFTER INVESTIGATION, IT WAS FOUND THAT THERE WAS A RUPTURE AND LEAKAGE IN THE STRAIGHT HEAD FILTER. CHANGE THE NEW ONE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23051660 ↗MalfunctionJan 30, 2025Fracture; Gas/Air Leak; Fracture; Gas/Air Leak
IT WAS REPORTED THAT: "(B)(6) 2024, DURING THE TEST, IT WAS FOUND THAT THERE WAS AN AIR LEAKAGE, AND THE PRODUCT WAS FOUND TO HAVE A FRACTURE. REPLACED WITH A NEW PRODUCT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21272385 ↗MalfunctionOct 18, 2021Break; Break
IT WAS REPORTED THAT "THE NURSE FOUND THE TUBE BROKEN WHEN USING ON PATIENT WHICH CAUSED LEAKING". NO INJURY OR HARM REPORTED. PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12647054 ↗
Other CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE) devices
- DAR 353S19046Covidien LP · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)1 recall1 report
- HUDSON RCI IPN042781Teleflex Incorporated · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)1 recall1 report
- DAR 354/5876Covidien LP · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)25 reports
- AVANOS 93816Avanos Medical, Inc. · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)24 reports
- HUDSON RCI IPN040673Teleflex Incorporated · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)11 reports
- Portex C45031682D-NLIcu Medical, Inc. · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)8 reports
- Portex 450952-NLIcu Medical, Inc. · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)8 reports
- HUDSON RCI IPN044386Teleflex Incorporated · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)7 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 · each recall links to the FDA recall notice
- 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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