3M™ Ranger™ 24370Recalls & reported problems
3m Company · 3M™ Ranger™ Blood/Fluid Warming High Flow Set, 24370, 10/Case · Class 2
All models of 3M Ranger (3)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10707387792708), received between Dec 17, 2023 and Apr 7, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (8 reports).
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.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak8
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 7, 2026Fluid/Blood Leak
A USER FACILITY REPORTED FOUR 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SETS LEAKED BLOOD AT THE CONNECTION OF THE TUBING AND CASSETTE. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24800570 ↗MalfunctionApr 6, 2026Fluid/Blood Leak
A USER FACILITY REPORTED FOUR 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SETS LEAKED BLOOD AT THE CONNECTION OF THE TUBING AND CASSETTE. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24795343 ↗MalfunctionApr 1, 2026Fluid/Blood Leak
A USER FACILITY REPORTED A 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET LEAKED BLOOD AT THE BUBBLE TRAP DURING USE. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24761033 ↗MalfunctionDec 11, 2025Fluid/Blood Leak; Fluid/Blood Leak
A USER FACILITY REPORTED A 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET LEAKED AT THE CASSETTE. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23785371 ↗MalfunctionMay 28, 2025Fluid/Blood Leak; Fluid/Blood Leak
A USER FACILITY REPORTED A 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET LEAKED WHILE PRIMING WITH SALINE, PRIOR TO PATIENT USE. THE LEAK WAS OBSERVED FROM THE BACK OF THE OUTLET PORT OF THE CASSETTE. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22099442 ↗MalfunctionMar 13, 2025Fluid/Blood Leak; Fluid/Blood Leak
A USER FACILITY REPORTED AT LEAST FIVE 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SETS LEAKED AT THE SECTION OF TUBING ON THE PATIENT SIDE OF THE BUBBLE TRAP. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21599430 ↗MalfunctionAug 21, 2024Fluid/Blood Leak; Fluid/Blood Leak
A USER FACILITY REPORTED THE 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET LEAKED DURING USE. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION. THE CUSTOMER LATER REPORTED THE LEAK WAS AT THE BUBBLE TRAP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20014061 ↗MalfunctionMar 29, 2024Leak/Splash; Leak/Splash
A USER FACILITY REPORTED 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET LEAKED AT THE HEAT EXCHANGER PORT AREA. NO INJURIES OR MEDICAL INTERVENTIONS WERE REPORTED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19004448 ↗MalfunctionDec 17, 2023Fluid/Blood Leak; Fluid/Blood Leak
A USER FACILITY REPORTED DURING A TRANSFUSION IN THE OPERATING ROOM, 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET, 24370, FAILED AT THE HUB JUST BELOW THE BUBBLE TRAP. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18342283 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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