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E SERIES 50011810020064013Recalls & reported problems

Zoll Medical Corporation · Defibrillator ,MAIN, AED-2, 12 LEAD, SPO2/SPCO/ETCO2/NIBP, GPS/BT, AC, NO RAILS, DMST · Class 3

All models of E SERIES (160)

Data updated Oct 16, 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 00847946017828), received between Feb 6, 2018 and Feb 6, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Power Up” (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 16, 2026.

Most reported problems

Device problems

  • Failure to Power Up1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionFeb 6, 2018Failure to Power Up; Failure to Power Up

    COMPLAINANT ALLEGED THAT DURING FUNCTIONAL TESTING, THE DEVICE WOULD INTERMITTENTLY NOT POWER UP. COMPLAINANT DID NOT INDICATE THAT THERE WAS ANY PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.

    Patient problems: No Patient Involvement

    MAUDE report 7245326 ↗

Other Automated external defibrillators (non-wearable) devices

All Automated external defibrillators (non-wearable) devices →

Sources and updates

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