Recall database

Prosthesis, Spinous Process Spacer/Plate recalls

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

Showing 1–1 of 1 recalls

Class IIOngoingZ-2485-2025

Boston Scientific Neuromodulation Corporation recalls Superion IDS Kit Superion Indirect Decompression System 8MM

As a result of a comprehensive product performance review it was determine that the device and instruments are not consistently meeting expected performance levels.…

Spinous Process Spacer/Plate Prosthesis
Device Design

Boston Scientific Neur…CASep 10, 2025