NeuroMAUDE
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Arrow International Agba Picc/Delta FG

No active recall

Manufacturer: Arrow International  · FDA product code: LJS  · Category: Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

Severity Snapshot

74 total reports2019-032024-06 date range6.8% physician / facility reported93.2% manufacturer reported1 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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