fda_recall · device_recall · high
Angiodynamics, Inc. — Class II recall: Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 N…
- Event date
- 2026-04-29 00:00:00Z
- Observed
- 2026-07-09 22:53:02Z
- Source ID
- Z-1857-2026
- Payload hash
- e0194f26664e544ceb6f91e0…
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.