Spencer Probe Depth Electrode RD10R-SP05X-000 (UDI 00841823108920)Recalls & reported problems
Ad-Tech Medical Instrument Corporation · Class 2
All models of Spencer Probe Depth Electrode (16)
Data updated Oct 18, 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 00841823108920), received between May 1, 2024 and May 1, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Signal Artifact/Noise” (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.
Reports received per month
Most reported problems
Device problems
- Signal Artifact/Noise1
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.
MalfunctionMay 1, 2024Signal Artifact/Noise; Signal Artifact/Noise
ON APRIL 16,2024 AN ELECTRODE WAS PLACED IN A PATIENT. THE ELECTRODE WAS TESTED IN THE OPERATING ROOM AND SHOWED ARTIFACT HOWEVER IT WAS DECIDED TO LEAVE IT IMPLANTED. ON (B)(6) 2024 DUE TO THE INCREASING AMOUNT OF ARTIFACT THE PATIENT WAS TAKEN BACK TO THE OR FOR A SECOND SURGERY TO REPLACE THE ELECTRODE. THERE WAS NO NEGATIVE EFFECT ON THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19220602 ↗
Other ELECTRODE, DEPTH devices
- Spencer Probe Depth Electrode SD04R-AP58X-000Ad-Tech Medical Instrument Corporation · ELECTRODE, DEPTH1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- Spencer Probe Depth Electrode SD06R-AP58X-000Ad-Tech Medical Instrument Corporation · ELECTRODE, DEPTH1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 reports
- NA MICRODEEP DEPTH ELECTRODEDixi Medical · Electrode, Depth1 recall0 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.
How reports and recalls are matched · Editorial policy · Report an error on this page