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Bard Per-Q-Cath Plus
No active recall
Manufacturer: Bard · FDA product code: LJS · Category: Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Severity Snapshot
445 total reports2005-08 – 2024-08 date range0% physician / facility reported0% manufacturer reported71 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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