AirLife 2050G-50Recalls & reported problems
Salter Labs · Salter Labs Oxygen Tubing (Green) with 2 standard connectors (6 mm), 50' (15.2 m) · 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 00607411200632), received between Jun 15, 2022 and Jun 15, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Twisted/Bent” (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.
Most reported problems
Device problems
- Material Twisted/Bent1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 15, 2022Material Twisted/Bent
THE TUBING COILS AND CAUSED A PATIENT TO FALL. THE END USER STATED HE HAS CHANGED HIS TUBING MULTIPLE TIMES AND CONTINUES TO HAVE ISSUES WITH IT COILING. HE ORDERS THROUGH APRIA AND VITALITY MEDICAL. THE PATIENT FELL AND ENDED UP IN THE HOSPITAL BECAUSE HE TRIPPED OVER THE TUBING.
Patient problems: Fall
MAUDE report 14701685 ↗
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- Flow sensor 155500Hamilton Medical AG · Tubing, Pressure And Accessories2 reports
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- 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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