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NA TCD-5-3MRecalls & reported problems

Boston Scientific Neuromodulation Corporation · Disposable TC Electrode, 5cm, 3m Cable · Class 2

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 00813250014358), received between Aug 11, 2017 and Aug 11, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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.

Most reported problems

Device problems

  • Break1
  • Material Discolored1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 11, 2017Break; Material Discolored; Break; Material Discolored

    A REPORT WAS RECEIVED THAT AN ELECTRODE SHAFT IS BROKEN FROM THE HUB.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6788585 ↗

Other PROBE, RADIOFREQUENCY LESION devices

All PROBE, RADIOFREQUENCY LESION devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.