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DigiTrak XT DigiTrak XT Holter RecorderRecalls & reported problems

Philips Medical Systems Hsg · DigiTrak XT Holter Recorder · Class 2

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 00884838000476), received between Aug 16, 2019 and Aug 16, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Patient Data Problem” (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

  • Patient Data Problem1

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.

  • MalfunctionAug 16, 2019Patient Data Problem

    CUSTOMER REPORTED THEY RECEIVED THE RECORDER BACK WITH THE WRONG PATIENT NAME. THERE WAS NO PATIENT INVOLVED.

    Patient problems: No Patient Involvement

    MAUDE report 8903131 ↗

Other ELECTROCARDIOGRAPH,AMBULATORY(WITHOUT ANALYSIS) devices

All ELECTROCARDIOGRAPH,AMBULATORY(WITHOUT ANALYSIS) devices →

Sources and updates

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