FDAOctober 12, 2022device

Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm

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

The hazard

Due to Indirect Decompression System devices exhibiting a potential for weld breakage at the spindle cap-to-main body interface. As a result of the separation of the spindle cap from the main body it may prevent proper deployment of the device during implantation.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientific neuromodulationbostonboston scientific

UPCs

008846620005290088466200054300884662000550

Recall history

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

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Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm — Recall Details · AllClear