# Major Recall Alert: Sentiva® Generator Recalled Due to Reed Switch Component Issue
In a critical update to a previously issued recall, Livanova has announced a follow-up recall for its **model 1000 Sentiva™** and **model 1000-D Sentiva Duo™ VNS Therapy™ generators**, addressing ongoing concerns related to the device’s **reed switch component issue**. The initial recall, identified as FA-NM-HOU-2024-00, was issued in January 2025. Following **Health Canada approval on July 15, 2025**, Livanova will now distribute updated devices with a design fix and remove all affected generators remaining in hospital inventory. The official recall starts on **August 11, 2025**.
**[H2] Why This Recall is Important**
This recall addresses a defect in the reed switch component of the Sentiva® Generator, which could cause malfunction or unreliability in the device. The **reed switch** is a crucial element in ensuring the proper internal mechanisms of the VNS Therapy™ generators. A defect in this component raises potential health risks for patients relying on the device’s consistent performance for therapy.
Failing to address this issue could compromise patient safety, further underscoring the importance of Livanova’s decision to recall and replace all affected models still in hospital inventory promptly. Additionally, the updated design for Sentiva™ generators has received regulatory clearance, ensuring a safer, more reliable alternative is available.
**[H3] Details of the Recall**
Here are the key details you need to know:
- **Product Name**: Sentiva® Generator
- **Recalled Models**: Model 1000 Sentiva™ and Model 1000-D Sentiva Duo™ VNS Therapy™ generators
- **Recall Start Date**: August 11, 2025
- **Issue**: Reed switch component defect may cause device malfunction.
- **Approval for Updated Models**: Health Canada approvals were issued on July 15, 2025.
- **Next Steps by Manufacturer**: Livanova will remove and replace all affected devices in hospital inventory and distribute updated versions of the Sentiva™ generator.
For more information on this specific recall, visit the **official source link**: [Health Canada Recall Announcement](https://recalls-rappels.canada.ca/en/alert-recall/sentivar-generator).
**[H3] What You Should Do**
If you or a loved one currently relies on a Sentiva® or Sentiva Duo™ VNS Therapy™ generator for therapy, here are the recommended actions:
- **Patients**: Contact your healthcare provider to confirm whether your device is impacted by the recall. Your physician will likely provide guidance on next steps, which may include monitoring your device’s performance or replacing it.
- **Healthcare Providers**: Check your hospital’s inventory against the recall notification. Livanova will coordinate the removal of affected generators and distribute the updated models.
Taking immediate action ensures patients remain safe and continue to receive therapy without interruption.
**[H3] Stay Safe – Get Instant Recall Alerts**
Keeping track of product recalls is vital for protecting yourself and your family. Stay ahead of the latest recall updates by downloading our app today! With instant notifications and detailed alerts, you’ll always be informed about potential risks in your products.
**🔗 [Download Our App Now](#) to Stay Safe and Alert.**
For more official information, visit the [Health Canada Recall Announcement page](https://recalls-rappels.canada.ca/en/alert-recall/sentivar-generator).
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