Clinician Programmer For Vercise™ Deep Brain Stimulation (dbs) Systems
Recall Summary Boston Scientific is recalling Clinician Programmer devices used with Vercise Deep Brain Stimulation systems across Canada due to a labeling or packaging defect. The recall is classified as Class II, meaning the defect could potentially cause adverse health effects but is not life-threatening. The issue affects the labeling or packaging rather than the device's function itself.
- Recalling firm
- Boston Scientific Neuromodulation Corporation
- Product
- Clinician Programmer for Vercise™ Deep Brain Stimulation (DBS) systems
- Reason
- Labelling or packaging defect
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-11-13
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/35c41597-fa68-4c81-b0cb-fdbf9db3a110