FDAJune 6, 2025device

Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect Decompression System 10MM, VF Implant 101-9810 00884662000536 Superion Indirect Decompression System 12MM, VF Implant 101-9812 00884662000543 Superion Indirect Decompression System 14...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

As a result of a comprehensive product performance review it was determine that the device and instruments are not consistently meeting expected performance levels. Issues include breakage of the instruments and implant/device.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientific neuromodulationbostonboston scientific

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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