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M SERIES CCT 40010811100024010Recalls & reported problems

Zoll Medical Corporation · Defibrillator ,MAIN CCT,MAN-2,3/5 LEAD,SPO2,NIBP,IBP,TEMP,BIPHSC,RCD,SMR,CDMK,AC,DMST · Class 2

All models of M SERIES CCT (10)

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 00847946004804), received between Apr 6, 2017 and Apr 6, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Operational Issue” (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

  • Device Operational Issue1

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.

  • MalfunctionApr 6, 2017Device Operational Issue; Device Operational Issue

    COMPLAINANT ALLEGED THAT DURING BIOMED TESTING THE DEVICE'S FRONT PANEL BUTTONS WERE UNRESPONSIVE WHEN THE DEVICE WAS IN DEFIB MODE. COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.

    Patient problems: No Patient Involvement

    MAUDE report 6464930 ↗

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Sources and updates

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