# **Major Recall Alert: HeartSine® Pad-Pak-07 Battery & Defibrillation Pads, HeartSine® Pad-Pak™, and HeartSine® Pediatric-Pak™ Recalled Due to Safety Concerns**
Attention, HeartSine Samaritan® PAD device users: a significant recall has been issued for HeartSine® Pad-Pak-07 Battery & Defibrillation Pads, HeartSine® Pad-Pak™, and HeartSine® Pediatric-Pak™. This recall, which began on **August 22, 2025**, stems from post-market surveillance findings indicating **improper insertion issues** that may lead to device failure during critical lifesaving operations.
Read on to learn why this recall is vital, detailed product information, steps you need to take, and how you can stay informed about safety updates.
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## **Why This Recall is Important**
Automated External Defibrillators (AEDs) like the HeartSine Samaritan® PAD devices are crucial for saving lives during sudden cardiac arrest. However, with the latest findings, the improper insertion of Pad-Paks into these devices due to:
- **Use error**
- **Bent locator pins** (potentially caused during manufacturing)
...poses a serious risk during emergencies.
### **Potential Consequences**:
1. **Device Connection Failure**: If the issue occurs, the device will repeatedly prompt, "apply pads to patient's bare chest."
2. **Device Malfunction**: In some cases, the AED may fail to power on entirely.
Such failures could delay or prevent critical treatment, directly jeopardizing lives. Addressing this recall is essential to ensure reliability during emergencies and maintain public safety.
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## **Details of the Recall**
The recall affects the following products under the **HeartSine®** brand:
- **HeartSine® Pad-Pak-07 Battery & Defibrillation Pads**
- **HeartSine® Pad-Pak™**
- **HeartSine® Pediatric-Pak™**
**Issue Identified**: Post-market surveillance revealed that the devices’ Pad-Paks may not always align properly during insertion, contrary to the **Instructions for Use (IFU)** provided. The root cause of the improper alignment includes user-related errors and flawed locator pins from manufacturing processes.
**Impact**: Improper alignment can lead to the device being unable to establish necessary connections, rendering it non-functional during an emergency.
**Recall Start Date**: August 22, 2025
For official details and updates, visit the official recall notice from Health Canada here: [HeartSine® Pad-Pak Recall Information](https://recalls-rappels.canada.ca/en/alert-recall/heartsiner-pad-paktm).
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## **What You Should Do**
If you own or manage AEDs with HeartSine® Pad-Pak products, take the following steps immediately:
- **Check Affected Products**: Identify if your device uses HeartSine® Pad-Pak-07, HeartSine® Pad-Pak™, or HeartSine® Pediatric-Pak™.
- **Review Device Operation**: Follow the Instructions for Use (IFU) for proper installation. Be mindful of issues such as resistance when inserting or visible bending of the locator pins.
- **Contact Manufacturer or Distributor**: Reach out for replacement parts or further guidance. Manufacturers typically provide detailed support during recalls to ensure consumer safety.
- **Train Users**: Ensure all AED operators are trained on proper Pad-Pak insertion to reduce user error risks during emergencies.
By taking proactive measures, you can substantially reduce risks and ensure the functionality of these lifesaving devices.
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## **Stay Safe – Get Instant Recall Alerts**
Safety is paramount, especially when it comes to lifesaving devices like AEDs. Stay up to date with recalls and product safety alerts immediately by downloading our free safety app. You'll receive personalized notifications for product recalls, keeping you informed and prepared.
[**Download the App Now!**]
For more detailed information about this recall, visit: [HeartSine® Pad-Pak Recall Information](https://recalls-rappels.canada.ca/en/alert-recall/heartsiner-pad-paktm).
Your vigilance can make all the difference in ensuring the safety and functionality of critical medical equipment. Stay informed and take action today!