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E SERIES 80001310020164013Recalls & reported problems

Zoll Medical Corporation · Defibrillator ,MAIN, AED-3, 12 LEAD, SPO2/ETCO2, BT/GPS, PACE, AC, NO RAILS, DMST,REFURB · Class 3

All models of E SERIES (160)

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 00847946015312), received between Aug 20, 2015 and Aug 20, 2015 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loss of Power” (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

  • Loss of Power1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionAug 20, 2015Loss of Power

    COMPLAINANT ALLEGED THAT WHILE ATTEMPTING TO TREAT A PT, THE DEVICE RESTARTED/REBOOTED ON ITS OWN. COMPLAINANT INDICATED THAT THE CLINICIAN RE-INSERTED THE BATTERIES AND POWERED THE DEVICE ON WHICH REMEDIED THE PROBLEM. COMPLAINANT INDICATED THAT THERE WAS NO ADVERSE EFFECT TO THE PT DUE TO THE REPORTED MALFUNCTION.

    Patient problems: No Information

    MAUDE report 5048855 ↗

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Sources and updates

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