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Jaeger V-175423-13Recalls & reported problems

Jaeger Medical GmbH · MasterScreen Body/Diff · Class 2

Data updated Oct 16, 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 04250892905181), received between Feb 24, 2020 and Feb 24, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Temperature 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 16, 2026.

Most reported problems

Device problems

  • Temperature 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.

  • MalfunctionFeb 24, 2020Temperature Problem; Temperature Problem

    THE CUSTOMER REPORTED A BURNING SMELL FROM THE CABIN. THERE WAS NO SMOKE AND THE BODY WAS FUNCTIONING. THERE WAS NO PATIENT INVOLVEMENT ASSOCIATED ON THIS EVENT.

    Patient problems: No Patient Involvement

    MAUDE report 9747180 ↗

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Sources and updates

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