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NA RFK-C10520SRecalls & reported problems

Boston Scientific Neuromodulation Corporation · Cannula, 10cm, 5mm tip, 20G Sharp Curved · 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 00813250012033), received between Jan 6, 2022 and Jan 6, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Markings/Labelling 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Markings/Labelling Problem1
  • Device Misassembled During Manufacturing /Shipping1

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.

  • MalfunctionJan 6, 2022Device Markings/Labelling Problem; Device Misassembled During Manufacturing /Shipping; Device Markings/Labelling Problem; Device Misassembled During Manufacturing /Shipping

    IT WAS REPORTED THAT THE FACILITY RECEIVED FOUR INCORRECTLY LABELED BOXES OF CANNULAS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13183450 ↗

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.