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BD Intima-Ii 22GAX1
No active recall
Manufacturer: BD · FDA product code: FOZ · Category: Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Severity Snapshot
86 total reports2019-05 – 2026-03 date range100% physician / facility reported0% manufacturer reported8 SKU variants
Failure & Consequence Profiles
Top Failure Modes
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Top Patient Outcomes
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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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