NeuroMAUDE
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Quickset 1PC Flex Drill Bit 35

No active recall

FDA product code: HTW  · Category: Bit, Drill

Severity Snapshot

847 total reports2008-042026-02 date range40.7% physician / facility reported59.3% manufacturer reported1 SKU variants

Reporting Trend

Annual Reporting Volume

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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.

Reported Events

Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.

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