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E SERIESRecalls & reported problems across all models

Zoll Medical Corporation · 160 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
833
Deaths reported
4
Injuries reported
0
Recalls
0

We found 160 models of E SERIES by Zoll Medical Corporation in the FDA's device registry (GUDID). Together they are named in 833 adverse event reports in the FDA's MAUDE database, received between Aug 3, 2015 and Mar 23, 2021 — classified as 4 deaths, 828 malfunctions.

The most frequently reported specific device problem is “Failure to Power Up” (503 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported E SERIES problems

Device problems

  • Failure to Power Up503
  • No Display/Image74
  • Device Displays Incorrect Message67
  • Failure of Device to Self-Test54
  • Defibrillation/Stimulation Problem25
  • Device Operational Issue20
  • Loss of Power17
  • Unable to Obtain Readings16

Patient problems

  • No Patient Involvement751
  • No Information53
  • No Consequences Or Impact To Patient14
  • No Known Impact Or Consequence To Patient7
  • Death4
  • Cardiac Arrest3
  • Atrial Fibrillation1
  • Insufficient Information1

E SERIES models

160 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.

Recent E SERIES adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Zoll Medical Corporation products

All Zoll Medical Corporation devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page