AirLife 2025G-25Recalls & reported problems
Salter Labs · Salter Labs Oxygen Tubing (Green) with 2 standard connectors (6 mm), 25’ (7.6 m) · 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 00607411200649), received between May 12, 2023 and Sep 20, 2025 — classified as 2 malfunctions.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Disconnection1
- Obstruction of Flow1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Numbness1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 20, 2025Obstruction of Flow; Obstruction of Flow
IT WAS REPORTED: TUBING IS TOO SOFT AND PINCHING OFF AT THE CONCENTRATOR; THE ISSUE CAUSED BACK FLOW OF OXYGEN TO THE CONCENTRATOR, CAUSING ALARMS AND LACK OF OXYGEN FLOW TO THE PATIENT. A NON-SERIOUS (UNSPECIFIED) INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23103389 ↗MalfunctionMay 12, 2023Disconnection; Disconnection
"SEPARATED WHERE THE TUBING MEETS THE CONNECTOR."THE FIRST OCCASION RESULTED IN NUMBNESS IN MY EXTREMITIES BEFORE I NOTICED THE DISCONNECTION AND COULD HAVE BEEN DEADLY HAD I GONE TO SLEEP WITHOUT DISCOVERING THE PROBLEM."
Patient problems: Numbness
MAUDE report 16919107 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.