HUDSON RCI IPN913839Recalls & reported problems
Teleflex Incorporated · Adult ConchaSmart Noninvasive Breathing Circuit with ConchaSmart column and Bacterial/Viral Filter · Class 2
All models of HUDSON RCI (152)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 14026704660473), received between Jul 30, 2021 and Aug 20, 2021 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Mechanical Problem” (6 reports).
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.
Most reported problems
Device problems
- Mechanical Problem6
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 20, 2021Mechanical Problem; Mechanical Problem
IT WAS REPORTED "WHEN THEY USE THE CIRCUITS WITH THIS LOT NUMBER, THE VENT THROWS AN ALARM UNTIL THE CIRCUIT IS CHANGED TO ONE NOT FROM THIS LOT NUMBER. PT CARE IS NOT AFFECTED EXCEPT BY THE ALARM NOISE. NO CLINICAL DETERIORATION". PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12348377 ↗MalfunctionAug 20, 2021Mechanical Problem; Mechanical Problem
IT WAS REPORTED "WHEN THEY USE THE CIRCUITS WITH THIS LOT NUMBER, THE VENT THROWS AN ALARM UNTIL THE CIRCUIT IS CHANGED TO ONE NOT FROM THIS LOT NUMBER. PT CARE IS NOT AFFECTED EXCEPT BY THE ALARM NOISE. NO CLINICAL DETERIORATION". PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12347205 ↗MalfunctionAug 20, 2021Mechanical Problem; Mechanical Problem
IT WAS REPORTED "WHEN THEY USE THE CIRCUITS WITH THIS LOT NUMBER, THE VENT THROWS AN ALARM UNTIL THE CIRCUIT IS CHANGED TO ONE NOT FROM THIS LOT NUMBER. PT CARE IS NOT AFFECTED EXCEPT BY THE ALARM NOISE. NO CLINICAL DETERIORATION". PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12347202 ↗MalfunctionAug 20, 2021Mechanical Problem; Mechanical Problem
IT WAS REPORTED "WHEN THEY USE THE CIRCUITS WITH THIS LOT NUMBER, THE VENT THROWS AN ALARM UNTIL THE CIRCUIT IS CHANGED TO ONE NOT FROM THIS LOT NUMBER. PT CARE IS NOT AFFECTED EXCEPT BY THE ALARM NOISE. NO CLINICAL DETERIORATION". PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12347111 ↗MalfunctionAug 20, 2021Mechanical Problem; Mechanical Problem
IT WAS REPORTED "WHEN THEY USE THE CIRCUITS WITH THIS LOT NUMBER, THE VENT THROWS AN ALARM UNTIL THE CIRCUIT IS CHANGED TO ONE NOT FROM THIS LOT NUMBER. PT CARE IS NOT AFFECTED EXCEPT BY THE ALARM NOISE. NO CLINICAL DETERIORATION". PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12347098 ↗MalfunctionJul 30, 2021Fracture; Mechanical Problem; Fracture; Mechanical Problem
IT WAS REPORTED "WHEN THEY USE THE CIRCUITS WITH THIS LOT NUMBER, THE VENT THROWS AN ALARM UNTIL THE CIRCUIT IS CHANGED TO ONE NOT FROM THIS LOT NUMBER. PT CARE IS NOT AFFECTED EXCEPT BY THE ALARM NOISE. NO CLINICAL DETERIORATION". PATIENT CONDITION REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12256670 ↗
Other Humidifier nebulizer kit devices
- HUDSON RCI HUD88015KITMedline Industries, Inc. · Humidifier nebulizer kit1 recall15 reports
- HUDSON RCI IPN913730Teleflex Incorporated · Humidifier nebulizer kit1 recall1 report
- Seattle PAP plus MP02260Drägerwerk AG & Co. KGaA · Humidifier Nebulizer Kit1 recall0 reports
- HUDSON RCI HUD88013KITMedline Industries, Inc. · Humidifier nebulizer kit1 recall0 reports
- HUDSON RCI IPN913731Teleflex Incorporated · Humidifier nebulizer kit1 recall0 reports
- HUDSON RCI HUD88014KITMedline Industries, Inc. · Humidifier nebulizer kit1 recall0 reports
- HUDSON RCI HUD88017KITMedline Industries, Inc. · Humidifier nebulizer kit1 recall0 reports
- HUDSON RCI HUD78001KITMedline Industries, Inc. · Humidifier nebulizer kit1 recall0 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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