Nanostim Leadless Cardiac Pacemaker (2017-11-17)
NANOSTIM Leadless Cardiac Pacemaker Recall The NANOSTIM Leadless Cardiac Pacemaker is being recalled in Canada due to safety concerns with the medical device. This recall affects pacemakers that were distributed across Canada. The FDA classified this as a Class I recall, indicating a serious health risk associated with the device.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-12-08
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/3d0e6cb3-fe5f-4228-ad7c-c93e14fb7319