# Major Recall Alert: FRED Easyport Recalled Due to Defective IGBT Modules, Effective April 1, 2025
Schiller Ag, a trusted name in medical equipment, has issued an urgent recall for the **FRED Easyport** due to defective IGBT modules. This defect can limit the device's ability to deliver life-saving shocks, posing a significant safety risk. With the recall starting April 1, 2025, those with this device must take immediate action to ensure their equipment is safe and effective.
Learn all the key details below and find out what steps you should take to address this recall.
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## Why This Recall is Important
The **FRED Easyport** is a portable defibrillator designed to save lives during cardiac emergencies. However, Schiller Ag has discovered a critical flaw in the device: defective **IGBT (Insulated Gate Bipolar Transistor) modules**. These modules are vital in ensuring the proper functioning of the device by enabling it to deliver a high number of electrical shocks reliably.
If the IGBT module malfunctions, the device may only deliver **a limited number of shocks** before failing. In life-threatening situations where every second counts, this malfunction could have serious or even fatal consequences. As a result, Schiller Ag has initiated this recall to address the defect and ensure the safety of users and patients.
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## Details of the Recall
Here’s what you need to know about the **FRED Easyport recall**:
- **Product Name**: FRED Easyport
- **Brand**: Schiller Ag
- **Category**: Medical Devices, Portable Defibrillators
- **Recall Reason**: Defective **IGBT modules** causing potential failure in delivering shocks.
- **Safety Concern**: Malfunctioning devices may not provide the required number of shocks during cardiac emergencies.
- **Recall Start Date**: April 1, 2025
- **Official Announcement Date**: [Link provided to recall page](https://recalls-rappels.canada.ca/en/alert-recall/fred-easyport-0)
This recall highlights the importance of ensuring critical medical devices are functioning properly. Users of the FRED Easyport are strongly encouraged to take immediate steps to address this issue.
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## What You Should Do
If you own or use a **FRED Easyport** portable defibrillator, it’s essential to act quickly. Follow these steps to ensure your safety or the safety of your patients:
1. **Check Your Device**: Determine if your FRED Easyport is affected by the defective IGBT module.
2. **Contact the Manufacturer**: Reach out to **Schiller Ag** or your local distributor for guidance on how to proceed. The manufacturer will provide instructions for servicing, repairing, or replacing the defective module.
3. **Stop Using the Device**: Avoid using affected devices until recommended safety measures are completed.
4. **Spread the Word**: Share this recall information with colleagues, healthcare facilities, or anyone who may own or use the FRED Easyport.
For additional information, consult the official recall page here: [FRED Easyport Recall](https://recalls-rappels.canada.ca/en/alert-recall/fred-easyport-0).
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## Stay Safe – Get Instant Recall Alerts
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Schiller Ag’s recall of the **FRED Easyport** is a critical reminder of the importance of routine maintenance and proactive safety checks on life-saving devices. Act now to address this recall and share these details with others who may be affected.