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
- Level 1 8002950Icu Medical, Inc. · Warmer, blood, non-electromagnetic radiation10 deaths931 reports
- Ranger™ 243553m Company · Warmer, blood, non-electromagnetic radiation107 reports
- 3M™ Ranger™ 243553m Company · Warmer, blood, non-electromagnetic radiation64 reports
- Ranger™ 243703m Company · Warmer, blood, non-electromagnetic radiation38 reports
- Ranger™ 243653m Company · Warmer, blood, non-electromagnetic radiation16 reports
- 3M™ Ranger™ 243703m Company · Warmer, blood, non-electromagnetic radiation9 reports
- buddy™ Disposable Set (1 Piece) 905-00010PBelmont Instrument Corporation · Warmer, Blood, Non-Electromagnetic Radiation8 reports
- °M Warmer System - °M Warmer MWS201Mequ A/S · Warmer, Blood, Non-Electromagnetic Radiation5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.