MasimoSET® Red DCI-dc12 SpO2 Adult Reusable Sensor 2054Recalls & reported problems
Masimo Corporation · MasimoSET Red DCI-dc12 SpO2 Adult Reusable Sensor · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00843997001243), received between Mar 4, 2021 and Aug 24, 2023 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Sensing Intermittently” (6 reports).
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
- Sensing Intermittently6
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 24, 2023Sensing Intermittently; Sensing Intermittently
THE CUSTOMER REPORTED SENSORS SUDDENLY STOPPED WORKING. NO PATIENT IMPACT OR CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17620168 ↗MalfunctionJan 12, 2023Sensing Intermittently; Sensing Intermittently
THE CUSTOMER REPORTED THAT THE SENSOR SUDDENLY STOPPED WORKING. NO CONSEQUENCES OR IMPACT TO PATIENT WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16152646 ↗MalfunctionMay 14, 2021Sensing Intermittently; Sensing Intermittently
THE CUSTOMER REPORTED THE SENSOR STOPS WORKING SUDDENLY. NO PATIENT IMPACT OR CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11826312 ↗MalfunctionMay 14, 2021Sensing Intermittently; Sensing Intermittently
THE CUSTOMER REPORTED THE SENSOR STOPS WORKING SUDDENLY. NO PATIENT IMPACT OR CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11826299 ↗MalfunctionMar 4, 2021Sensing Intermittently; Sensing Intermittently
THE CUSTOMER REPORTED THAT THE SENSORS SUDDENLY STOPPED WORKING. NO CONSEQUENCES OR IMPACT TO PATIENT WERE REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 11417894 ↗MalfunctionMar 4, 2021Sensing Intermittently; Sensing Intermittently
THE CUSTOMER REPORTED THAT THE SENSORS SUDDENLY STOPPED WORKING. NO CONSEQUENCES OR IMPACT TO PATIENT WERE REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 11417878 ↗
Other Oximeter devices
- Trilogy Trilogy100 Ventilator, InternationalRespironics, Inc. · Oximeter8 deaths2,493 reports
- Trilogy Trilogy 202 Ventilator, United StatesRespironics, Inc. · Oximeter2 deaths1,594 reports
- HAMILTON-G5 159001Hamilton Medical AG · Oximeter18 deaths1,440 reports
- Trilogy Trilogy100 Ventilator, GermanyRespironics, Inc. · Oximeter696 reports
- Model EMV+ Vent, Army, MRI 799-EMVP-04Zoll Medical Corporation · Oximeter1 death605 reports
- Trilogy Evo, O2, Japan JP2100X16BRespironics, Inc. · Oximeter4 recalls5 deaths342 reports
- Model EMV+ Vent, Army, COMMERCIAL 799-EMVP-01-01Zoll Medical Corporation · Oximeter1 death497 reports
- HAMILTON-G5 159002Hamilton Medical AG · Oximeter3 deaths451 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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