N/A 4950-7-7Recalls & reported problems
Salter Labs · Salter Labs™ Adult. EtCO2/O2 Nasal Divided Cannula, male luer style CO2 connector. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00607411301681), received between Jul 13, 2017 and Apr 25, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Connection 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Connection Problem1
- Incomplete or Inadequate Connection1
- Misassembled1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 25, 2025Connection Problem; Incomplete or Inadequate Connection; Connection Problem; Incomplete or Inadequate Connection
PRODUCT WILL NOT STAY CONNECTED WHEN RUNNING A PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21914551 ↗MalfunctionJul 13, 2017Misassembled; Misassembled
INITIAL AND FINAL REPORT. CUSTOMER REPORTS THE OXYGEN TUBING LEAKED WHICH APPEARED TO CAUSE A PATIENT'S O2 SATURATION TO DROP (VALUE NOT SUPPLIED). THE PATIENT RESPONDED TO SUPPLEMENTAL O2 BY THE NURSE ANESTHETIST. THE CANNULA WAS CHANGED AND THE PROCEDURE WAS COMPLETED WITHOUT FURTHER INCIDENT. PATIENT WAS DISCHARGED TO HOME AFTER AN UNEVENTFUL RECOVERY. THERE WAS NO INJURY REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6712803 ↗
Other ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE devices
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- BD Alaris™ ETCO2 Module, Model 8300Carefusion 303, Inc. · ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE485 reports
- BD Alaris™ ETCO2 Module, Model 8300Carefusion 303, Inc. · ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE471 reports
- NA GF-210RNihon Kohden Corporation · ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE386 reports
- Trilogy IT2110X21BRespironics, Inc. · ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE5 recalls30 reports
- Trilogy Trilogy Evo Ventilator, GermanyRespironics, Inc. · ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE5 recalls26 reports
- Trilogy Evo Trilogy Evo Ventilator with oxygen blending model, GermanyRespironics, Inc. · ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE5 recalls9 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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