NeuroMAUDE
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Abbott Guidant

No active recall

Manufacturer: Abbott  · FDA product code: DQX  · Category: Wire, Guide, Catheter

Severity Snapshot

26 total reports1999-082012-07 date range0% physician / facility reported0% manufacturer reported4 SKU variants

Reporting Trend

Annual Reporting Volume

Click any bar to view those reports ↓

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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