Abre Venous Self-expanding Stent System
Abre Venous Self-Expanding Stent System Recall Medtronic Inc. is recalling the Abre Venous Self-Expanding Stent System across Canada due to a device performance issue. The stent is used to treat venous conditions. This is a Class II recall, meaning the device may not work as intended but serious injury is not likely.
- Recalling firm
- Medtronic Inc.
- Product
- Abre Venous Self-Expanding Stent System
- Reason
- Device performance issue
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-10-26
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1b10d436-1472-45b8-a186-ee1c7494fd47