MasimoSET Red LNC-04 LNCS® Patient Cable 2055Recalls & reported problems
Masimo Corporation · MasimoSET Red LNC-04 LNCS Patient Cable · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00843997001250), received between Jul 30, 2017 and Sep 9, 2022 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Incorrect Measurement” (2 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
- Incorrect Measurement2
- Device Stops Intermittently1
- Sensing Intermittently1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 9, 2022Sensing Intermittently; Sensing Intermittently
THE CUSTOMER REPORTED INTERMITTENT READINGS. NO PATIENT IMPACT OR CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15396289 ↗MalfunctionJun 30, 2021Incorrect Measurement; Incorrect Measurement
THE CUSTOMER REPORTED A FAILURE TO GET READINGS AND/OR ACCURATE READINGS. NO PATIENT IMPACT OR CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12096389 ↗MalfunctionJul 30, 2017Incorrect Measurement; Device Stops Intermittently; Incorrect Measurement; Device Stops Intermittently
THE CUSTOMER REPORTED OVER THE PAST 2 MONTHS, THEY HAVE BEEN ACQUIRING MORE AND MORE FAILED CABLE PARTS - EITHER THROUGH OUTRIGHT CABLE FAILURES AS PRESENTED ON THE ZOLL UNIT ITSELF, TO INCONSISTENT READINGS TO NO READINGS WHAT-SO-EVER. NO PATIENT IMPACT OR CONSEQUENCES WERE REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6753128 ↗
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- 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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