Aveir™ Leadless Pacemaker
Aveir™ Leadless Pacemaker Recall Summary Abbott is recalling Aveir™ Leadless Pacemakers across Canada due to a device compatibility issue. This is a Class I recall, the most serious classification. The recall affects pacemakers that were distributed throughout Canada.
- Product
- Aveir™ Leadless Pacemaker
- Reason
- Device compatibility
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-08-19
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/6c37e010-bd33-40cf-b482-2a5d9621b7d4