N/A 1606BRecalls & reported problems
Salter Labs · Nasal Cannula (Adult) Salter Style without supply tube · Class 1
- 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 00607411102004), received between Dec 24, 2025 and Dec 24, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Chemical Problem” (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
- Chemical Problem1
Patient problems
- Caustic/Chemical Burns1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 24, 2025Chemical Problem; Chemical Problem
A STRONG CHEMICAL SMELL WAS NOTED AFTER OPENING THE PACKAGING, THE PATIENT USED THE CANNULA AND RECEIVED CHEMICAL BURNS TO THEIR NOSE (SORES IN THE NOSE) AFTER USE. THERE WAS NO REPORT OF MEDICAL INTERVENTION; NO INFORMATION PROVIDED CONCERNING THE PATIENT'S OUTCOME.
Patient problems: Caustic/Chemical Burns
MAUDE report 23891230 ↗
Other CANNULA, NASAL, OXYGEN devices
- Fisher & Paykel Healthcare OPT844Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen39 reports
- Fisher and Paykel Healthcare OPT312Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen22 reports
- Fisher and Paykel Healthcare OPT314Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen17 reports
- O2 Cannula 001366Salter Labs · Cannula, Nasal, Oxygen10 reports
- O2 Cannula 001365Salter Labs · Cannula, Nasal, Oxygen9 reports
- N/A 16SOFT-4Salter Labs · CANNULA, NASAL, OXYGEN8 reports
- N/A 1053-7Salter Labs · CANNULA, NASAL, OXYGEN8 reports
- Fisher & Paykel Healthcare OPT842Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen7 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.