ZOLL recalls Powerheart G5 AED models G5A-00A to G5A-80A-TSO due to potential failure in self-tests from extreme temperatures or humidity. No action needed if device is in normal use conditions.
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
ZOLL is recalling Powerheart G5 AED models with serial numbers starting with D00000177884 to D00000015030 for possible self-test failures in extreme temperatures or humidity. This does not pose a risk if the device is used in normal conditions.
The device may fail its self-test function when exposed to extreme temperatures or humidity over time, which could lead to incorrect operation during a cardiac emergency. However, this is not a risk in normal use conditions.
Owners of Powerheart G5 AEDs with model numbers G5A-00A through G5A-80A-TSO and serial numbers listed in the recall notice are affected. Emergency responders and first aid users are most at risk if the device is exposed to extreme temperatures or humidity.
Check for model numbers G5A-00A to G5A-80A-TSO on the device. The serial numbers listed in the recall notice (starting with D00000177884) indicate affected units. The device is designed for use in normal conditions.
Verify the model number on the device to see if it matches G5A-00A through G5A-80A-TSO.
Check the serial number against the list provided in the recall notice to determine if the device is affected.
No, the device is safe for normal use in typical conditions. The risk only occurs with prolonged exposure to extreme temperatures or humidity.
If your device's model and serial number are not on the recall list, no action is required.
Check the model number and serial number against the list of affected models and serial numbers provided in the recall notice.
We’ve drafted a message you can send ZOLL to request your refund or repair — edit it as you like.
Subject: Recall Z-1316-2025 — ZOLL ZOLL Hello, I own a ZOLL that is covered by recall Z-1316-2025 from ZOLL. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
