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Voluntary Recall Notice: HeartSine Samaritan PAD AEDs

HeartSine Samaritan PAD is a small, lightweight, portable, battery-operated Automated External Defibrillator (AED) designed to treat victims of cardiac arrest.

HeartSine Technologies has announced a voluntary recall for a specific subset of its Samaritan PAD models due to a manufacturing issue that could impair the device’s ability to function or cause it to fail during use.

Affected Models

The recall applies to the following models:

  • 350P

  • 360P

  • 450P

  • 500P

Only devices with serial numbers starting with 21, 22, 23, or 24, followed by the letters B, D, E, G, or H, are affected.

Potential Risk

If affected, the device may fail to deliver the intended therapy, which could delay or prevent treatment during a cardiac arrest emergency.

How to Check if Your AED is Affected

To confirm whether your device is part of the recall, visit the official HeartSine recall page and enter your device’s serial number: HeartSine Recall Checker

Manufacturer Guidance

The manufacturer advises keeping your HeartSine Samaritan PAD in service if you do not have an alternative public access defibrillator. This is based on internal testing showing a low probability of failure due to the manufacturing issue.
If you have questions or need advice about AED safety and replacements, please contact the Qualsafe Shop team:
📞 0330 660 0599
📧 sales@qualsafe.com
Voluntary Recall Notice: HeartSine Samaritan PAD AEDs

HeartSine Samaritan PAD is a small, lightweight, portable, battery-operated Automated External Defibrillator (AED) designed to treat victims of cardiac arrest.

HeartSine Technologies has announced a voluntary recall for a specific subset of its Samaritan PAD models due to a manufacturing issue that could impair the device’s ability to function or cause it to fail during use.

Affected Models

The recall applies to the following models:

  • 350P

  • 360P

  • 450P

  • 500P

Only devices with serial numbers starting with 21, 22, 23, or 24, followed by the letters B, D, E, G, or H, are affected.

Potential Risk

If affected, the device may fail to deliver the intended therapy, which could delay or prevent treatment during a cardiac arrest emergency.

How to Check if Your AED is Affected

To confirm whether your device is part of the recall, visit the official HeartSine recall page and enter your device’s serial number: HeartSine Recall Checker

Manufacturer Guidance

The manufacturer advises keeping your HeartSine Samaritan PAD in service if you do not have an alternative public access defibrillator. This is based on internal testing showing a low probability of failure due to the manufacturing issue.
If you have questions or need advice about AED safety and replacements, please contact the Qualsafe Shop team:
📞 0330 660 0599
📧 sales@qualsafe.com

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