Recall database

Probe, Radiofrequency Lesion recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–3 of 3 recalls

Class IIOngoingZ-2694-2026

Boston Scientific Neuromodulation Corporation recalls Intracept Access Instruments

Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to severe infection.

Radiofrequency Lesion Probe
Packaging process control

Boston Scientific Neur…CAJul 15, 2026

Class IIOngoingZ-2403-2026

Boston Scientific Neuromodulation Corporation recalls Boston Scientific TCN Electrodes: REF: TCN-5

Reusable electrodes may not meet expected performance levels.

Radiofrequency Lesion Probe
Under Investigation by firm

Boston Scientific Neur…CAJun 17, 2026

Class IIOngoingZ-2402-2026

Boston Scientific Neuromodulation Corporation recalls Boston Scientific CSK Electrodes: REF: CSK-TC10

Reusable electrodes may not meet expected performance levels.

Radiofrequency Lesion Probe
Under Investigation by firm

Boston Scientific Neur…CAJun 17, 2026