MEDLINE INDUSTRIES, INC. HCSU4507Recalls & reported problems
Medline Industries, Inc. · TUBING,OXYGEN,CRUSH RES,7',CLEAR,UC · Class 1
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 10884389966105), received between Sep 1, 2026 and Sep 1, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Disconnection” (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
- Disconnection1
Patient problems
- Low Oxygen Saturation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 1, 2026Disconnection
It was reported that ¿Patients extension tubing disconnected from itself at 2019¿ and ¿patients¿ extension tubing disconnected.¿
Patient problems: Low Oxygen Saturation
MAUDE report 50545595 ↗
Other TUBING, PRESSURE AND ACCESSORIES devices
- O2 Cannula 001350Salter Labs · Tubing, Pressure And Accessories93 reports
- AirLife 2002-7Salter Labs · TUBING, PRESSURE AND ACCESSORIES6 reports
- AirLife SO-1968-0Salter Labs · TUBING, PRESSURE AND ACCESSORIES3 reports
- O2 Tubing 001304USalter Labs · Tubing, Pressure And Accessories3 reports
- AirLife SO-1188-0Salter Labs · TUBING, PRESSURE AND ACCESSORIES3 reports
- Flow sensor 155500Hamilton Medical AG · Tubing, Pressure And Accessories2 reports
- AirLife 2025G-25Salter Labs · TUBING, PRESSURE AND ACCESSORIES2 reports
- HUDSON RCI HUD1115Medline Industries, Inc. · TUBING, PRESSURE AND ACCESSORIES2 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.
How reports and recalls are matched · Editorial policy · Report an error on this page