ZOLL recalls Powerheart G5 AED model G5S-80C due to potential failure in extreme temperatures or humidity. Affected units have serial numbers listed in the recall. No injuries reported; users should check if their device is affected and follow the recall instructions.
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 devices with model number G5S-80C because they may fail their self-test when exposed to extreme temperatures or humidity. This could lead to the device not working properly during emergencies. The recall does not involve injuries or deaths, but users should check if their device is affected and follow the instructions.
The device may fail its self-test when exposed to extreme temperatures or humidity over time. This could cause the AED to not function properly during a cardiac emergency, potentially delaying life-saving treatment.
Owners of Powerheart G5 AED devices with model G5S-80C and the listed serial numbers are affected. Emergency responders and individuals with home AEDs are most at risk if they use the device in extreme conditions.
Check if your Powerheart G5 AED has model number G5S-80C and serial numbers listed in the recall (e.g., D00000171086, D00000171087, etc.). The device is designed for home or emergency use.
Verify your Powerheart G5 AED has model number G5S-80C and one of the listed serial numbers.
If your device is affected, contact ZOLL Medical Corporation for further instructions.
This recall is low risk. The device may fail its self-test in extreme temperatures or humidity, but no injuries have been reported. The hazard does not cause immediate harm.
Check if your Powerheart G5 AED has model number G5S-80C and a serial number listed in the recall (e.g., D00000171086, D00000171087, etc.).
No action is needed if your device is not affected by this recall.
We’ve drafted a message you can send ZOLL to request your refund or repair — edit it as you like.
Subject: Recall Z-1321-2025 — ZOLL ZOLL Hello, I own a ZOLL that is covered by recall Z-1321-2025 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.
