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Ranger™ 24500Recalls & reported problems

3m Company · 3M™ Ranger™ Fluid Warming Unit, Model 245, 120V-ENG-E , 1 each, 24500 · Class 2

All models of Ranger (10)

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 00707387781491), received between Feb 17, 2023 and Feb 17, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

  • Device Contamination with Chemical or Other Material1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionFeb 17, 2023Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

    A FACILITY REPORTED A BLOWN CONTROLLER WITH BURN MARKS ON THE INTERIOR CASING AND CONTROLLER OF 3M¿ RANGER¿ FLUID WARMING UNIT, MODEL 245 UPON OPENING THE UNIT FOR SERVICE BY THEIR TECHNICIAN. NO OTHER OBSERVATIONS WERE DISCOVERED WHILE IN USE. NO MEDICAL INTERVENTIONS WERE REQUIRED. NO PATIENT OR STAFF INJURY WAS ALLEGED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16396832 ↗

Other Warmer, blood, non-electromagnetic radiation devices

All Warmer, blood, non-electromagnetic radiation devices →

Sources and updates

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