fda_recall · device_recall · high
Angiodynamics, Inc. — Class II recall: AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers;…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:53Z
- Source ID
- Z-1873-2026
- Payload hash
- 4c57672e0da298d737c47fb4…
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.