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Ranger™ 24355 (UDI 50608223243553)Recalls & reported problems

3m Company · 3M™ Ranger® Fluid Warming Set, High Flow, 10 Per Case 24355 · Class 2

Adverse event reports
6
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 50608223243553), received between Nov 22, 2017 and Jul 11, 2018 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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

  • Appropriate Device Problem Term/Code Not Available5
  • Fluid/Blood Leak1

Patient problems

  • Not Applicable6

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 11, 2018Fluid/Blood Leak; Fluid/Blood Leak

    A HOSPITAL EMPLOYEE REPORTED USE OF A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET. THE EMPLOYEE ALLEGED THAT THE WARMING UNIT LEAKED SALINE FLUID AT THE AT THE LUER CONNECTION AREA. A PHOTO OF THE PRODUCT WAS PROVIDED WHICH REFLECTED A Y-CONNECTOR SOLVENT BOND LEAK. THE LEAK WAS DISCOVERED, DURING PRIMING, PRIOR TO BEING USED ON A PATIENT. THE FLUID WAS BEING WARMED AT 15-20 DEGREES CELSIUS. A PRESSURE INFUSOR WAS BEING USED AT THE TIME. NO PATIENT INJURY WAS ALLEGED.

    Patient problems: Not Applicable

    MAUDE report 7679368 ↗
  • MalfunctionMay 22, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    A HOSPITAL EMPLOYEE REPORTED USE OF A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET. THE EMPLOYEE ALLEGED THAT THE WARMING UNIT LEAKS FLUID AT THE "Y" CONNECTOR TUBING ON TOP PERIODICALLY. NO PATIENT INJURY WAS ALLEGED.

    Patient problems: Not Applicable

    MAUDE report 7534294 ↗
  • MalfunctionApr 26, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    IT WAS ALLEGED THAT A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET LEAKED FLUID AT THE AT THE "Y" CONNECTOR TUBING ON TOP. NO INJURY WAS ALLEGED.

    Patient problems: Not Applicable

    MAUDE report 7466262 ↗
  • MalfunctionApr 26, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    IT WAS ALLEGED THAT A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET LEAKED FLUID AT THE DRIP CHAMBER. NO INJURY WAS ALLEGED.

    Patient problems: Not Applicable

    MAUDE report 7466257 ↗
  • MalfunctionFeb 15, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    IT WAS ALLEGED THAT A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET LEAKED WHERE IT SPIKES UNDERNEATH AT THE "Y" CONNECTION. NO INJURY WAS ALLEGED.

    Patient problems: Not Applicable

    MAUDE report 7273448 ↗
  • MalfunctionNov 22, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    IT WAS ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET LEAKED WITHIN THE MIDDLE OF THE CASSETTE PORTION OF THE HEAT EXCHANGER. NO INJURY WAS REPORTED. TYPE OF FLUID BEING USED WAS NOT SPECIFIED.

    Patient problems: Not Applicable

    MAUDE report 7054335 ↗

Other Warmer, blood, non-electromagnetic radiation devices

All Warmer, blood, non-electromagnetic radiation devices →

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