Vercise Genus™ R 16 And R32 Implantable Pulse Generator Kits
Vercise Genus™ R 16 and R32 Implantable Pulse Generator Kits Recall Boston Scientific is recalling Vercise Genus™ R 16 and R32 Implantable Pulse Generator Kits across Canada due to a performance issue with the devices. These are implanted devices used to deliver electrical stimulation for treating movement disorders. The recall affects all patients in Canada who have received these specific pulse generator models.
- Product
- Vercise Genus™ R 16 and R32 Implantable Pulse Generator Kits
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-07-18
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1c33b5f5-ed9e-45e9-b5ff-8510424ba954