# Major Recall Alert: PowerEase Handpiece Recalled Due to Device Wobble Issue
Medtronic has issued an urgent voluntary recall of specific serial numbers of the **IPC PowerEase system (model number: 2300000)**. The affected products, sold under the **PowerEase Handpiece** brand, have been reported to experience **out-of-box failures**, specifically **device wobble**. This safety concern, first reported on **July 17, 2025**, has prompted a proactive recall to safeguard users.
This recall highlights the importance of addressing potential risks in medical devices, ensuring patient and healthcare personnel safety. Read on for the full details and what steps you should take.
## Why This Recall is Important
When it comes to medical equipment, reliability is non-negotiable. Medtronic—a trusted name in the industry—initiated this recall after receiving reports of performance failure. The **PowerEase Handpiece** is an integral tool in surgical procedures, and even minor malfunctions such as **device wobble** can have serious implications.
This proactive recall is being conducted in collaboration with health regulatory authorities to eliminate risks associated with the affected serial numbers. It serves as a reminder of the importance of vigilance in monitoring and reporting potential issues with critical medical devices.
## Details of the Recall
Medtronic officially announced the voluntary recall to address **out-of-box failure** reports received for the **PowerEase Handpiece (model number: 2300000)**. Here’s what you need to know:
- **Product Name**: PowerEase Handpiece
- **Model Number**: 2300000
- **Recall Reason**: Out-of-box device wobble during use
- **Recall Start Date**: July 17, 2025
- **Manufacturer**: Medtronic
- **Country**: Canada (CAN)
- **Affected Users**: Healthcare providers and facilities using the IPC PowerEase system
For those who own or operate this device, Medtronic has stated that action should be taken immediately to identify whether your device falls under the specific serial numbers affected by this recall.
## What You Should Do
If you or your healthcare facility uses the **PowerEase Handpiece**, follow these steps to ensure safety:
1. **Inspect the Device**: Verify if your **PowerEase Handpiece (model: 2300000)** is part of the recall by checking the serial number.
2. **Cease Use Immediately**: If your serial number matches, stop using the device to avoid potential issues.
3. **Contact Medtronic**: Reach out to Medtronic’s support team for guidance on how to return or replace the affected handpiece.
4. **Monitor Official Updates**: Stay informed by regularly checking updates issued by Health Canada or Medtronic.
For more information, please visit the official recall notice here: [PowerEase Handpiece Recall Notice](https://recalls-rappels.canada.ca/en/alert-recall/powerease-handpiece).
## Stay Safe – Get Instant Recall Alerts
Recalls like this can affect not only healthcare professionals but also the patients who rely on critical devices for safe and effective treatment. To ensure you stay on top of recalls for medical devices and other products, consider using a recall tracking app.
With the **[My Recalls App](https://myrecalls.app)**, you can:
- Receive **instant alerts** on product recalls.
- Access product-specific recall details with images and instructions.
- Protect yourself and others from potential risks.
Where your health is concerned, every second counts. **Download the My Recalls App** today and never miss an important update.
Stay informed. Stay safe.