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Hi-Torque Balance Middleweight Universal Guide Wire
No active recall
FDA product code: DQX · Category: Wire, Guide, Catheter
Severity Snapshot
479 total reports2002-05 – 2024-03 date range10.1% physician / facility reported89.9% 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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