MasimoSET LNC-10 LNCS® Series Patient Cable 1814Recalls & reported problems
Masimo Corporation · MasimoSET LNC-10 LNCS Series Patient Cable · Class 2
Data updated Oct 18, 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 00843997000512), received between Mar 24, 2017 and Jul 16, 2017 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Sensing 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 18, 2026.
Most reported problems
Device problems
- Device Sensing Problem1
- Incorrect Measurement1
Patient problems
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 16, 2017Incorrect Measurement; Incorrect Measurement
THE CUSTOMER REPORTED FLUCTUATIONS SPO2 MEASUREMENT. NO CONSEQUENCES OR IMPACT TO PATIENT WAS REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6716544 ↗MalfunctionMar 24, 2017Device Sensing Problem; Device Sensing Problem
IT WAS REPORTED THAT THE DEVICE WORKS INTERMITTENTLY. PER THE CUSTOMER, "THE USER REPORTS THAT THE SPO2 MEASUREMENT ENDS DURING OPERATION. RE-CONNECTING OR REPLACING THE INTERMEDIATE CABLE WITH THE INFINITY M540 ELIMINATES THE FAILURE. THE FINGER SENSOR FLASHES DURING THE FAILURE. THIS ERROR OCCURS SPORADICALLY ON SEVERAL M540S AND ALSO WITH SEVERAL INTERMEDIATE CABLES." NO KNOWN IMPACT OR CONSEQUENCE TO PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6434497 ↗
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- 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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