FDAMay 12, 2023device

Driver Instrument, part of the Superion Indirect Decompression System, REF: 102-9800, used with the Superion Indirect Decompression System IFU, Superion IDS Kit IFU, Surgical Technique Manual

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

The hazard

Pending update to indirect decompression system instructions for use informing users that excessive force during the implant procedure may cause driver instrument tip breaks, which may result in metal fragments (Driver teeth/tips) within the implant location; and if metal fragments are not removed and remain in situ, MRI scans are NOT advised due to potential risk of patient injury.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientific neuromodulationbostonboston scientific

UPCs

00884662000574

Recall history

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

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