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Stryker Prowler Select
No active recall
Manufacturer: Stryker · FDA product code: QJP · Category: Catheter, Percutaneous, Neurovasculature
Severity Snapshot
395 total reports2025-06 – 2026-03 date range100% physician / facility reported0% manufacturer reported1 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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