O2 Tubing 001303URecalls & reported problems
Salter Labs · Oxygen Tubing 14 foot (4.3m) Crush-Resistant Lumen, Vynil Tipped and U/Connect-It Adapter · 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 10889483569832), received between Apr 30, 2026 and Apr 30, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Incomplete or Inadequate Connection” (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
- Incomplete or Inadequate Connection1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 30, 2026Incomplete or Inadequate Connection
IT WAS REPORTED, THE TUBING WAS EXTRA-LONG AND CONTINUALLY POPPED OFF THE OXYGEN FLOWMETER (ABOUT (FIVE) 5 DIFFERENT TIMES) WHILE BAGGING [THE PATIENT] DURING A CODE; THE TUBING WAS REPLACED. MINIMAL TEMPORARY HARM WAS REPORTED; HOWEVER, THERE WAS NO REPORTED INJURY AS A RESULT OF THIS REPORTED EVENT.
Patient problems: Insufficient Information
MAUDE report 25046268 ↗
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.
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