fda_recall · device_recall · high
Angiodynamics, Inc. — Class II recall: AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-V…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:58Z
- Source ID
- Z-1875-2026
- Payload hash
- c9c58a0b0c7c7544910063c6…
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.