HUDSON RCI HUD87098KITRecalls & reported problems
Medline Industries, Inc. · CONCHASMART CIRCUIT, ADLT, NIV, SL, HTD · Class 2
All models of HUDSON RCI (30)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10197344010950), received between Oct 22, 2025 and Sep 29, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Melted” (2 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.
Reports received per month
Most reported problems
Device problems
- Melted2
- Fire1
- Smoking1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Melted
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938026 ↗MalfunctionOct 22, 2025Fire; Melted; Smoking; Fire; Melted; Smoking
ACCORDING TO THE FACILITY, "(B)(6) NOTICED SMOKE ON THE BED, OPENED THE BLANKET AND FOUND BLUE TUBINGS FROM THE BIPAP ON FIRE AND MELTING. BIPAP MACHINE NOT ON PER RN." FACILITY REPORTS NO INJURIES OR IMPACT TO PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23358677 ↗
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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