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Intellisense® Battery Powerheart® G5 XBTAED001ARecalls & reported problems

Zoll Medical Corporation · Intellisense non-rechargeable battery for Powerheart G5 AED with 4 year full replacement guarantee · Class 3

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00812394020904), received between Oct 28, 2019 and Oct 28, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unintended Electrical Shock” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Unintended Electrical Shock1

Patient problems

  • Complaint, Ill-Defined1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 28, 2019Unintended Electrical Shock; Unintended Electrical Shock

    THE DISTRIBUTOR REPORTED THEY WERE CONTACTED BY A CUSTOMER WHO REPORTED TO THEM THAT WHEN ONE OF THEIR SITE NURSES WAS INSTALLING A BATTERY IN AN AED SHE HAD HER FINGER ACROSS THE METAL CONDUCTION NOTCHES OF THE BATTERY AND IT SHOCKED HER. THE NURSE WAS REPORTED TO BE FINE, BUT DID FEEL "OFF" SO THE SCHOOL CALLED EMS AND SHE WAS TRANSPORTED TO THE HOSPITAL TO BE CHECKED OUT, ESPECIALLY SINCE SHE WAS PREGNANT.

    Patient problems: Complaint, Ill-Defined

    MAUDE report 9244728 ↗

Other Automated External Defibrillators (Non-Wearable) devices

All Automated External Defibrillators (Non-Wearable) devices →

Sources and updates

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