Nellcor PMC10NCH-GERecalls & reported problems
Covidien LP · GE ApexPro (TM) CH SpO2 - Nellcor Cable;For use with GE Patient Monitors. · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 10884521780699), received between Apr 9, 2024 and Apr 9, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Alarm System” (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
- Device Alarm System1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 9, 2024Device Alarm System; Device Alarm System
ACCORDING TO THE REPORTER, POST-OPERATIVELY, WHEN THE SPO2 WENT INTO "X" STATE WHEN THE SPO2 WAS NOT ON THE PATIENT, THE USER DID NOT RECEIVE A "PROBE OFF" ALARM. AS A RESULT, THE USER WAS NOT AWARE THAT SP02 WAS NOT BEING MONITORED. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19071640 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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