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Medline MDSPHY100LORecalls & reported problems

Medline Industries, Inc. · PAD,DEFIB,ADULT,RADIOLUCENT,PHYSIO,LO · Class 2

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 10888277635012), received between Sep 1, 2023 and Sep 1, 2023 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Temperature Problem1

Patient problems

  • Burn(s)1

Recent adverse event reports

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

  • InjurySep 1, 2023Temperature Problem; Temperature Problem

    PAD CAUSED A PATIENTS BEARD TO CATCH FIRE.

    Patient problems: Burn(s)

    MAUDE report 17672488 ↗

Other Electrode, electrocardiograph, multi-function devices

All Electrode, electrocardiograph, multi-function devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.