Back to home
Penumbra Solitaire
No active recall
Manufacturer: Penumbra · FDA product code: NRY · Category: Catheter, Thrombus Retriever
Severity Snapshot
382 total reports2009-11 – 2026-03 date range55.1% physician / facility reported44.9% manufacturer reported3 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…