Back to Stryker
Stryker Phenom Catheter
No active recall
Manufacturer: Stryker · FDA product code: QJP · Category: Catheter, Percutaneous, Neurovasculature
Severity Snapshot
331 total reports2023-09 – 2026-03 date range97.6% physician / facility reported2.4% manufacturer reported1 SKU variants
Reporting Trend
Annual Reporting Volume
Click any bar to view those reports ↓
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.
Loading reports…