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M SERIES CCTRecalls & reported problems across all models

Zoll Medical Corporation · 10 models in the FDA device registry

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

Adverse event reports
191
Deaths reported
3
Injuries reported
0
Recalls
0

We found 10 models of M SERIES CCT by Zoll Medical Corporation in the FDA's device registry (GUDID). Together they are named in 191 adverse event reports in the FDA's MAUDE database, received between Jul 31, 2015 and Nov 15, 2022 — classified as 3 deaths, 188 malfunctions.

The most frequently reported specific device problem is “Failure to Power Up” (48 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 M SERIES CCT problems

Device problems

  • Failure to Power Up48
  • Defibrillation/Stimulation Problem28
  • No Display/Image24
  • Device Displays Incorrect Message13
  • Device Operational Issue12
  • Pacing Problem12
  • Activation Problem11
  • Unable to Obtain Readings7

Patient problems

  • No Patient Involvement175
  • No Information8
  • No Consequences Or Impact To Patient3
  • Death2
  • Necrosis1
  • No Known Impact Or Consequence To Patient1
  • Premature Labor1

M SERIES CCT models

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

Recent M SERIES CCT 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