Absolute Pro Ll .035 Peripheral Self-expanding Stent System
Recall Summary Absolute Pro LL .035 Peripheral Self-Expanding Stent System devices are being recalled in Canada due to performance issues. The recall affects all units of this stent system that were distributed across Canada. This is classified as a Class I recall, indicating a serious issue with device performance.
- Product
- Absolute Pro Ll .035 Peripheral Self-Expanding Stent System
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-05-30
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/11cea196-00ee-4f23-914b-34d6aa3fb71e