# Major Recall Alert: Eterna™ Implantable Pulse Generator Recalled Due to Bluetooth® Communication Issues
Abbott has announced a significant recall for its **Eterna™ spinal cord stimulation (SCS) implantable pulse generators (IPGs), Model 32400**, following a potentially critical issue. These IPGs are experiencing communication failures with the clinician programmer (CP) and the patient controller (PC). This problem has been traced to a **Bluetooth® low energy (BLE) circuit component manufacturing defect**, raising concerns for patients reliant on this device for pain management.
To ensure your safety, learn more about the recall, how it impacts users, and immediate actions to take.
---
## Why This Recall is Important
Spinal cord stimulation devices like the **Eterna™ Implantable Pulse Generator** are life-changing tools for patients managing chronic pain. Abbott's Model 32400, however, has encountered a flaw that could compromise communication between the implant and its external controllers, including:
- **Clinician Programmer (CP):** Used by healthcare professionals to configure and adjust the device.
- **Patient Controller (PC):** Allows patients to monitor and control their comfort settings.
When a Bluetooth communication error occurs, patients may be unable to manage their therapy properly, leading to discomfort or disruptions in pain relief. For clinicians, the inability to access the device could hinder necessary updates or troubleshooting. This raises both health and safety concerns for affected patients.
Abbott is taking action by notifying healthcare providers and customers about this issue. If you use or know someone using an **Eterna™ spinal cord stimulation device**, it’s essential to follow the recommended safety measures.
---
## Details of the Recall
Key details about the recall include:
- **Brand Name:** Eterna™ Implantable Pulse Generator
- **Affected Model:** 32400
- **Issue:** Loss of Bluetooth® communication with CP and/or PC due to a circuit component defect in manufacturing.
- **Category:** Recall for spinal cord stimulation devices.
- **Date Announced:** October 2, 2023
- **Manufactured By:** Abbott
For official details, visit the Government of Canada recall page: [Eterna™ Implantable Pulse Generator Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/eternatm-implantable-pulse-generator).
---
## What You Should Do
If you, a loved one, or a patient is using the **Eterna™ Implantable Pulse Generator Model 32400**, follow these essential steps:
- Immediately contact your healthcare provider or clinician to confirm if your device is affected.
- Avoid attempting to recalibrate or troubleshoot the device on your own.
- Work actively with your clinician and Abbott representatives to discuss next steps, including potential replacement or fixes.
Abbott has initiated a notification campaign to ensure outreach, but it's advisable to act promptly if you suspect issues.
---
## Stay Safe – Get Instant Recall Alerts
Safety and health are critical, especially when medical devices like the **Eterna™ Implantable Pulse Generator** face potential malfunctions. Stay proactive and informed about recalls like this with ease by downloading our **recall notification app** today.
With the app, you’ll get:
- Real-time updates on recalls, including medical devices, food, and other safety alerts in Canada.
- Notifications delivered directly to your mobile device.
- Advice on how to take immediate action for affected products.
**Don’t wait – protect yourself and your loved ones today. Download the app and stay safe!**
---
For more official information about this recall, click the following link: [Eterna™ Implantable Pulse Generator Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/eternatm-implantable-pulse-generator).
Act now to ensure your safety and avoid potential disruption to your therapy. Share this post with family, friends, or colleagues who might be affected!