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LifeWatch Mobile Cardiac Telemetry 3-Lead MCT 3L-Brigadier-VerizonRecalls & reported problems

Lifewatch · 3 Lead Continuous ECG Monitor & Arrhythmia Detector (Brigadier/Android/Verizon) · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00850725007026), received between Jun 24, 2019 and Jun 24, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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

  • Insufficient Device Problem Information1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • InjuryJun 24, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    ON (B)(6) 2019, THE INITIAL REPORTED (PATIENT) NOTIFIED LIFEWATCH SERVICES, LLC ((B)(4)) THAT THE "DEVICE SHOCKED ME IN THE MIDDLE OF MY HEART". THE PATIENT INDICATED THAT THE SHOCK SENSATION WAS COMING FROM THE ELECTRODES. THE PATIENT DID NOT SEEK MEDICAL ATTENTION FOR THE ALLEGED EVENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8727309 ↗

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Sources and updates

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