# Major Recall Alert: Microdeep Depth Electrode Recalled Due to Manufacturing Defect in Caps
A significant recall has been issued for **Microdeep Depth Electrode** by **Dixi Medical** after the discovery of a **manufacturing defect** in the product’s caps. The defect affects the clamping function, which may compromise the safe positioning of the device. Customers are being urged to **immediately isolate any affected devices** to ensure patient safety. Below, we provide all the essential details about the recall and the steps you need to take.
---
## Why This Recall is Important
Patient safety is the top priority in all medical devices, and any equipment that fails to function as intended can lead to serious risks. This recall impacts **Microdeep Depth Electrodes**, which are critical in neurological diagnostics and treatments. Here's why this issue demands urgent attention:
- **Compromised Clamping Function**: It has been reported that the caps used in the electrodes might allow the electrodes to slip inside, even when the cap is screwed onto the guiding screw. This could hinder proper stabilization during medical procedures.
- **Potential Safety Risks**: With the clamping mechanism being ineffective, there is a possibility for improper positioning or device displacement, potentially putting patients at risk.
- **Isolation Needed**: Users are advised not to use affected devices and to isolate them to avoid accidental deployment.
The recall was officially announced on **July 30, 2025**, and is being closely monitored by healthcare regulators in Canada to ensure timely corrective measures are taken.
---
## Details of the Recall
Here are the key details regarding the **Microdeep Depth Electrode Recall**:
- **Product Involved**: Microdeep Depth Electrode
- **Brand**: Dixi Medical
- **Issue**: A defect in the caps used on the device, leading to a potential failure in the clamping mechanism, which may allow electrodes to slip
- **Category**: CAN (Canada) – Medical Device Recall
- **Recall Start Date**: July 30, 2025
For complete details, visit the official recall announcement on the Government of Canada’s website: [Microdeep Depth Electrode Recall](https://recalls-rappels.canada.ca/en/alert-recall/microdeep-depth-electrode).
---
## What You Should Do
If you or your healthcare facilities use **Microdeep Depth Electrodes**, it’s essential to act immediately:
- **Stop Using the Product**: Avoid using the affected devices to prevent any risks in patient treatment.
- **Isolate the Devices**: Separate all defective devices to ensure they are not accidentally used.
- **Contact Customer Support**: Reach out to the manufacturer, Dixi Medical, for further instructions, including possible replacements or repairs.
- **Check Recall Notices**: Stay updated by monitoring official recall notifications for the latest information.
---
## Stay Safe – Get Instant Recall Alerts
Medical device recalls like this highlight the importance of staying informed about potential risks. To ensure you always have the latest updates, consider downloading a **recall alert app** for real-time notifications. Stay one step ahead in safeguarding your health and safety.
---
The **Microdeep Depth Electrode Recall** is a clear reminder of how critical product functionality is in ensuring patient safety. If you own or use these devices, take necessary action now to mitigate risks. For official details and updates, visit the **Government of Canada recall page** [here](https://recalls-rappels.canada.ca/en/alert-recall/microdeep-depth-electrode).
Be proactive—protect your safety and that of others by staying informed!