Vanta Implantable Neurostimulator (ins)
Vanta Implantable Neurostimulator Recall Summary Medtronic is recalling the Vanta Implantable Neurostimulator (INS) devices in Canada due to a performance issue. This device is a surgically implanted unit used to deliver neurostimulation therapy. The recall affects all Vanta INS devices distributed across Canada and has been classified as Class I, indicating the most serious type of recall.
- Product
- Vanta Implantable Neurostimulator (INS)
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-08-26
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/4a822b1f-c14a-4247-8688-dfa147e5a287