ZOLL recalls Powerheart G5 AED models G5S-00A-TSO through G5S-90A due to potential self-test failure from prolonged exposure to extreme temperatures or humidity. No remedy is specified in the recall notice.
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 G5S-00A-TSO through G5S-90A because they may fail self-tests after prolonged exposure to extreme temperatures or humidity. This could affect the device's ability to properly detect cardiac emergencies. The recall does not include a specific remedy.
The devices may fail their self-test function when exposed to extreme temperatures or humidity over time. This could lead to the device not properly detecting cardiac emergencies, potentially delaying life-saving treatment.
Owners of Powerheart G5 AED models G5S-00A-TSO through G5S-90A are affected. Most at risk are individuals who use these devices in environments with high temperatures or humidity, such as outdoor settings or humid climates.
Check your Powerheart G5 AED for model numbers G5S-00A-TSO through G5S-90A. The device may have a serial number starting with 'D00000' or 'M00000' followed by numbers.
Look for the model number on the device, which should be one of G5S-00A-TSO through G5S-90A.
The recall notice does not specify any remedy or fix for this issue.
Check the model number on your Powerheart G5 AED; affected models are G5S-00A-TSO through G5S-90A.
No immediate action is required, but you should check if your device is affected before using it in extreme environments.
We’ve drafted a message you can send ZOLL to request your refund or repair — edit it as you like.
Subject: Recall Z-1322-2025 — ZOLL ZOLL Hello, I own a ZOLL that is covered by recall Z-1322-2025 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.
