C6 Sensor 2.5 rebuilt 02-01889Recalls & reported problems
Braemar Manufacturing, LLC · Class 2
Data updated Oct 16, 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 B146C6R10), received between Sep 25, 2023 and Sep 25, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fire” (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.
Most reported problems
Device problems
- Fire1
- Overheating of Device1
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.
MalfunctionSep 25, 2023Fire; Overheating of Device; Fire; Overheating of Device
THE PATIENT REPORTED THAT THEY LAID THE SENSOR ON AN ENVELOPE AND THE SENSOR BURNED THROUGH THE PAPER. THE SENSOR WAS NOT HOT PRIOR TO SETTING IT DOWN. THERE WAS NO HARM TO THE PATIENT REPORTED. THE SENSOR WAS REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17807540 ↗
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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 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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