AirLife SO-1188-0Recalls & reported problems
Salter Labs · Salter Labs TUBING KIT · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00607411889097), received between Apr 22, 2022 and Mar 5, 2024 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Appropriate Device Problem Term/Code Not Available1
- Insufficient Device Problem Information1
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Bruise/Contusion1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMar 5, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PATIENT FELL AND CAUGHT HIS FEET IN THE TUBING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18843072 ↗InjuryMar 1, 2024Material Twisted/Bent; Material Twisted/Bent
THE PATIENT CAUGHT HER FEET IN THE TUBE AND FELL: LARGE BRUISES ON THE RIGHT THIGH + A CRACKED RIB, HER CONDITION DID NOT REQUIRE HOSPITALIZATION.
Patient problems: Bruise/Contusion
MAUDE report 18822985 ↗MalfunctionApr 22, 2022Insufficient Device Problem Information
INFLAMMATION OF THE TUBING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14189567 ↗
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
- 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
- Medline HCS4550GBMedline 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