fda_recall · device_recall · high
Angiodynamics, Inc. — Class II recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACC…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:53:01Z
- Source ID
- Z-1874-2026
- Payload hash
- e56981300a7be22922d08fc9…
Summary
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Status: Ongoing.
Entities
Informational only. Not legal, financial, or medical advice.