HUDSON RCI HUD1115Recalls & reported problems
Medline Industries, Inc. · TUBING, OXYGEN, STAR LUMEN, 7 L, SC · Class 1
- 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 10197344042234), received between May 28, 2026 and Sep 2, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Gas/Air Leak” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Gas/Air Leak2
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 2, 2026Gas/Air Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50570977 ↗MalfunctionMay 28, 2026Gas/Air Leak
IT WAS REPORTED THAT THE O2 TUBING BEING USED FOR NEBULIZER HAD LEAK JUST BELOW CONNECTION TO O2.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25322300 ↗
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- AirLife 2025G-25Salter Labs · TUBING, PRESSURE AND ACCESSORIES2 reports
- Medline HCS4550GBMedline Industries, Inc. · TUBING, PRESSURE AND ACCESSORIES2 reports
- Flow sensor 155500Hamilton Medical AG · Tubing, Pressure And Accessories2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.