Ranger™ 24200 (UDI 50608223242006)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50608223242006), received between Jan 17, 2024 and Jan 17, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device 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

Recent adverse event reports

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

• InjuryJan 17, 2024Use of Device Problem; Use of Device Problem

  A USER FACILITY REPORTED A HYPOTHERMIC FEMALE PATIENT IN HER LATE 40'S WAS TRANSPORTED TO THE EMERGENCY ROOM.THE PATIENT WAS GIVEN A BOLUS AND 3M¿ RANGER¿ BLOOD/FLUID WARMING STANDARD FLOW SET, 24200 WAS INITIATED. IT WAS NOT IDENTIFIED IF THE BOLUS WAS GIVEN BEFORE INITIATING THE RANGER OR IF IT WAS GIVEN THROUGH THE RANGER SET. THE PATIENT WAS THEN TRANSFERRED TO COMPUTED TOMOGRAPHY (CT) WITH THE RANGER ATTACHED TO AN INTRAVENOUS (IV) LINE POLE WHERE A LARGE AMOUNT OF AIR IN THE VASCULAR SYSTEM WAS FOUND. THE PATIENT WAS TRANSFERRED TO A HOSPITAL FOR HYPERBARIC TREATMENT AND INTENSIVE CARE. THE PATIENT HAS BEEN DISCHARGED FROM THE HOSPITAL.

  Patient problems: Air Embolism

  MAUDE report 18530863 ↗