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Medline DYNJAER4009Recalls & reported problems

Medline Industries, Inc. · TEMPERATURE PROBE 9FR W/400 SERIES TEMP · Class 2

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10080196551705), received between Nov 16, 2021 and Nov 16, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Positioning 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

  • Positioning Problem1
  • Unintended Movement1

Patient problems

  • Insufficient Information2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 16, 2021Unintended Movement

    IT WAS REPORTED BY THE FACILITY THAT THE TEMPERATURE PROBE WAS INSERTED INTO THE PATIENT AND ENDED UP IN THE PATIENT'S RIGHT MAIN STEM. (PT. #2). NO ADDITIONAL INFORMATION IS AVAILABLE.

    Patient problems: Insufficient Information

    MAUDE report 12820365 ↗
  • InjuryNov 16, 2021Positioning Problem

    IT WAS REPORTED BY THE FACILITY THAT THE TEMPERATURE PROBE WAS INSERTED INTO THE PATIENT AND ENDED UP IN THE RIGHT MAIN STEM. NO ADDITIONAL INFORMATION IS AVAILABLE.

    Patient problems: Insufficient Information

    MAUDE report 12819945 ↗

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