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Hi-Torque Balance Middleweight Guide Wire

No active recall

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

Severity Snapshot

428 total reports1997-112022-08 date range1.2% physician / facility reported98.8% manufacturer reported3 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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