HUDSON RCI HUD88009KITRecalls & reported problems
Medline Industries, Inc. · CIRCUIT,ISO-GARD,INFANT,HTD,COLUMN,DRN · Class 2
All models of HUDSON RCI (30)
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 10197344010912), received between Sep 28, 2026 and Sep 28, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Overheating of Device” (1 report).
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
- Overheating of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Overheating of Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922134 ↗
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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