fda_recall · device_recall · high
Angiodynamics, Inc. — Class II recall: Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 N…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:52:54Z
- Source ID
- Z-1866-2026
- Payload hash
- 9ca31c9f5109a59945f36318…
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.