fda_recall · device_recall · high
Angiodynamics, Inc. — Class II recall: AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:54Z
- Source ID
- Z-1872-2026
- Payload hash
- ab16ec2677f5edef772f5e49…
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.