O2 Tubing 001305URecalls & reported problems
Salter Labs · Oxygen Tubing 25 feet (7.6m) Crush Resistant Oxygen Tubing, 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889483569894), received between Nov 6, 2025 and Nov 6, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
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.
InjuryNov 6, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT INABILITY TO REMOVE THREAD GRIP ADAPTER CAUSING THE O2 TUBING TO DETACH.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23493538 ↗
Other Tubing, Pressure And Accessories devices
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- 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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