Ranger™ 24365Recalls & reported problems
3m Company · 3M™ Ranger™ Fluid Warming Set, High Flow, AVBT Only, 10 per case 24365 · Class 2
All models of Ranger (10)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 16
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 16 adverse event reports that list this exact device (DI 50707387781465), received between Apr 22, 2019 and Dec 29, 2020 — classified as 16 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (16 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 18, 2026.
Most reported problems
Device problems
- Fluid/Blood Leak16
Patient problems
- Not Applicable16
Recent adverse event reports
The 16 most recent of 16 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 29, 2020Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) LEAKED AT THE SIDE OF THE CASSETTE. NO PATIENT/STAFF INJURY WAS ALLEGED. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Not Applicable
MAUDE report 11091443 ↗MalfunctionJul 14, 2020Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) BROKE AFTER SET UP. LOCATION OF THE BREAK WAS NOT AVAILABLE. NO PATIENT OR STAFF INJURY WAS REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Not Applicable
MAUDE report 10272967 ↗MalfunctionMar 18, 2020Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL REPORTED THE 3M¿ RANGER¿ BLOOD/FLUID WARMING SYSTEM HIGH FLOW WITH AUTO-VENTING BUBBLE TRAP MODEL 24365 LEAKED AT THE AUTO VENTING BUBBLE TRAP. TYPE OF LIQUID ALLEGED TO HAVE LEAKED WAS NOT SPECIFIED. NO PATIENT INJURY WAS ALLEGED. NO INFORMATION WAS PROVIDED AS TO IF THE SET WAS PRIMED PRIOR TO USE, OR IF A PRESSURE DEVICE WAS USED.
Patient problems: Not Applicable
MAUDE report 9849065 ↗MalfunctionFeb 4, 2020Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) LEAKED FLUID INSIDE A 3M¿ RANGER¿ WARMING UNIT. NO PATIENT OR STAFF INJURY WAS ALLEGED. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Not Applicable
MAUDE report 9664351 ↗MalfunctionJan 29, 2020Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) LEAKED FLUID AT THE SIDE OF THE FILTER. NO PATIENT/STAFF INJURY WAS ALLEGED. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Not Applicable
MAUDE report 9643870 ↗MalfunctionDec 26, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) LEAKED FLUID AT THE SIDE, NEAR THE FILTER. NO PATIENT/STAFF INJURY WAS ALLEGED. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Not Applicable
MAUDE report 9519822 ↗MalfunctionDec 16, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) LEAKED FLUID AROUND THE SIDE OF THE AUTO-VENTING BUBBLE TRAP. THE EMPLOYEE ALLEGED THE CASSETTE BURST WHILE A PATIENT (AGE/GENDER NOT SPECIFIED) WAS BEING RESUSCITATED. NO PATIENT INJURY WAS ALLEGED. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Not Applicable
MAUDE report 9473833 ↗MalfunctionNov 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) LEAKED FLUID FROM THE SIDE OF THE AUTO VENTING BUBBLE TRAP. THE EMPLOYEE ALLEGED SECOND SET WAS DISCOVERED TO HAVE A KINK BELOW THE AUTO VENTING BUBBLE TRAP. THE CASSETTE REPORTEDLY BURST INSIDE THE RANGER¿ WARMING UNIT. THE WARMING UNIT WAS SENT TO BIOMED. NO PATIENT OR STAFF INJURY WAS ALLEGED. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Not Applicable
MAUDE report 9309246 ↗MalfunctionNov 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED TWO 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SETS (MODEL 24365) LEAKED FLUID. ONE SET REPORTEDLY WAS DISCOVERED TO HAVE A KINK IN THE TUBING BELOW THE AUTO-VENTING BUBBLE TRAP. THE EMPLOYEE ALLEGED THAT SET LEAKED SALINE AT THE SEAM DURING PRIMING. THE EMPLOYEE ALLEGED A SECOND SET LEAKED SALINE AT THE SEAM BY THE AUTO-VENTING BUBBLE TRAP DURING PRIMING. NO PATIENT OR STAFF INJURY WAS ALLEGED.
Patient problems: Not Applicable
MAUDE report 9309244 ↗MalfunctionOct 29, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED TWO 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SETS (MODEL 24365) LEAKED SALINE FLUID DURING PRIMING ON (B)(6) 2019. THE SETS WERE REPORTEDLY PRIMED TO GRAVITY. ONE SET REPORTEDLY LEAKED SALINE FROM THE BUBBLE TRAP. THE SECOND SET REPORTEDLY LEAKED SALINE NEAR THE TUBING INSERTION INTO THE CASSETTE. NO PATIENT OR STAFF INJURY WAS ALLEGED.
Patient problems: Not Applicable
MAUDE report 9252114 ↗MalfunctionOct 28, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) LEAKED RBC FLUID NEAR THE BUBBLE TRAP DURING ADMINISTRATION ON (B)(6) 2019. A PERIPHERAL IV WAS USED FOR THE INFUSION. A BAXTER Y-TYPE BLOOD/SOLUTION SET WITH A LARGE STANDARD BLOOD FILTER AND PRESSURE PUMP WAS USED TO APPLY MANUAL/HAND PRESSURE. THE ANESTHESIA TEAM REPORTEDLY BECAME CONTAMINATED. THE PROCEDURE WAS REPORTEDLY DELAYED DUE TO THE REMOVAL AND REPLACEMENT OF THE BLOOD WARMING AND TRANSFUSION COMPONENTS. NO PATIENT OR STAFF INJURY WAS ALLEGED.
Patient problems: Not Applicable
MAUDE report 9244372 ↗MalfunctionOct 16, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) LEAKED FLUID FROM THE AUTO VENTING BUBBLE TRAP DURING PRIMING. NO PATIENT OR STAFF INJURY WAS ALLEGED.
Patient problems: Not Applicable
MAUDE report 9197461 ↗MalfunctionOct 14, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) LEAKED FLUID FROM THE AUTO VENTING BUBBLE TRAP DURING PRIMING. NO PATIENT OR STAFF INJURY WAS ALLEGED.
Patient problems: Not Applicable
MAUDE report 9186992 ↗MalfunctionSep 16, 2019Fluid/Blood Leak; Fluid/Blood Leak
AN ANESTHESIA ASSISTANT REPORTED A MALE PATIENT IN HIS 70'S WAS RESUSCITATED IN THE OPERATING ROOM ON (B)(6) 2019. THE PATIENT WAS BEING ADMINISTERED RBC FLUID VIA A 3M¿ RANGER¿ HIGH FLOW DISPOSABLE SET (MODEL 24365) WARMED BY A 3M¿ RANGER¿ WARMING UNIT (MODEL 24500). A LARGE GAUGE NEEDLE FOR THE CORDIS LINE WAS USED FOR INFUSION. MANUAL HAND PRESSURE WAS APPLIED. THE EMPLOYEE ALLEGED A FLUID LEAKED OCCURRED FROM THE SIDE OF THE AUTO VENTING BUBBLE TRAP DURING INFUSION. THE PATIENT'S CARE WAS REPORTEDLY DELAYED IN ORDER TO RE-ESTABLISH THE BLOOD INFUSION VIA AN ALTERNATE METHOD, A FMS BELMONT MACHINE. THE ANESTHESIOLOGIST WAS REPORTEDLY EXPOSED TO BLOOD. NO BLOOD CULTURES WERE DONE. NO STAFF INJURY WAS ALLEGED. THE FLUID WAS DRAINED PRIOR TO REMOVING THE SET FROM THE WARMING UNIT. THE EMPLOYEE REPORTED BIOMED CHECKED THE WARMING UNIT PRIOR TO BEING PUT INTO SERVICE. THE PATIENT IS REPORTEDLY STABLE.
Patient problems: Not Applicable
MAUDE report 9072181 ↗MalfunctionJun 24, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED A 3M¿ RANGER ¿ HIGH FLOW FLUID WARMING SET (MODEL 24365) LEAKED WHOLE BLOOD FROM THE OUTLET PORT ON THE HEAT EXCHANGER WHILE PREPPING FOR SURGERY. NO HARMFUL EXPOSURE TO BLOOD OR INJURY WAS ALLEGED.
Patient problems: Not Applicable
MAUDE report 8727691 ↗MalfunctionApr 22, 2019Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL EMPLOYEE ALLEGED THAT A 3M¿ RANGER ¿ HIGH FLOW FLUID WARMING SET (MODEL 24365) LEAKED WHOLE BLOOD FROM A CRACK IN THE BUBBLE TRAP WHILE PUMPING. FURTHER DETAILS REGARDING USAGE OF THE DEVICE WERE NOT SPECIFIED. NO PATIENT INJURY OR HARMFUL EXPOSURE TO BLOOD WAS ALLEGED.
Patient problems: Not Applicable
MAUDE report 8537468 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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