Nanostim Leadless Cardiac Pacemaker
Nanostim Leadless Cardiac Pacemaker Recall Abbott is recalling Nanostim leadless cardiac pacemakers in Canada because the devices may unexpectedly stop delivering pacing therapy due to a potential electrical issue. The recall affects patients who have received this pacemaker implant. This is a Class I recall, meaning there is a reasonable probability that use of the product will cause serious adverse health consequences or death.
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-11-07
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/8f8f07c7-2033-400e-8199-137e63499321