Urgent recall: HeartSine Samaritan AEDs may be defective

In June 2025, Stryker initiated a global recall for several HeartSine samaritan AED models: the 350P, 360P, 450P, and 500P. Internal investigation revealed that a defect in a printed circuit board component could lead to a malfunction during use, such as the failure or delay of a shock delivery when the AED is deployed.

Although there have been no reports of incidents during actual resuscitations to date, Stryker takes the risk seriously. According to the manufacturer, the risk of failure remains low. Users are advised to continue using their AEDs if no alternative is available, provided they are checked regularly.

Temporary unavailability of AEDs and PadPaks
Due to the recall, HeartSine samaritan AEDs and their associated PadPaks are currently unavailable. The expected delivery delay may last until the end of 2025. Please keep this in mind when replacing or servicing your equipment.

Check your AED
The recall affects AEDs with serial numbers beginning with 21, 22, 23, or 24, followed by the letters B, D, E, G, or H. The serial number can be found on the back of the device. Stryker advises you to monitor the status indicator closely while the AED is in use.

What to do?
- Check the serial number of your AED.
- Follow any instructions provided by Stryker or your supplier.
- Continue to visually inspect your AED until replacement occurs.

This measure underscores the importance of strict quality control for life-saving equipment. AEDwijzer is closely monitoring the situation and will inform users as soon as updates are available.

More information can be found on the official Stryker website:
www.stryker.com/nl/en/emergency-care/product-notices/heartsine/fa318-t3.html