RangerRecalls & reported problems across all models
3m Company · 10 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 176
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls
- 0
We found 10 models of Ranger by 3m Company in the FDA's device registry (GUDID). Together they are named in 176 adverse event reports in the FDA's MAUDE database, received between Mar 6, 2017 and May 16, 2025 — classified as 7 injuries, 169 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (159 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Ranger problems
Device problems
- Fluid/Blood Leak159
- Appropriate Device Problem Term/Code Not Available9
- Loss of Osseointegration4
- Material Integrity Problem2
- Connection Problem1
- Crack1
- Device Contamination with Chemical or Other Material1
- Device Operates Differently Than Expected1
Patient problems
- No Clinical Signs, Symptoms or Conditions108
- Not Applicable55
- Failure of Implant5
- Insufficient Information5
- Air Embolism2
- Inflammation1
- No Consequences Or Impact To Patient1
Ranger models
10 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Ranger™ 24355Warmer, blood, non-electromagnetic radiation107 reports
- Ranger™ 24370Warmer, blood, non-electromagnetic radiation38 reports
- Ranger™ 24365Warmer, blood, non-electromagnetic radiation16 reports
- Ranger™ 24355Warmer, blood, non-electromagnetic radiation6 reports
- Ranger™ 24533Warmer, blood, non-electromagnetic radiation4 reports
- Ranger™ 24500Warmer, blood, non-electromagnetic radiation1 report
- Ranger™ 24533Warmer, blood, non-electromagnetic radiation1 report
- Ranger™ 24200Warmer, blood, non-electromagnetic radiation1 report
- Ranger™ 24200Warmer, blood, non-electromagnetic radiation1 report
- Ranger™ 24200Warmer, blood, non-electromagnetic radiation1 report
Recent Ranger adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryMay 16, 2025Fracture; Fracture
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FRACTURE.
Patient problems: Failure of Implant
MAUDE report 22040123 ↗InjuryMay 16, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 22040041 ↗InjuryMay 16, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 22040034 ↗InjuryMay 16, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 22039982 ↗InjuryApr 17, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Inflammation
MAUDE report 21854303 ↗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 ↗MalfunctionFeb 17, 2023Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
A FACILITY REPORTED A BLOWN CONTROLLER WITH BURN MARKS ON THE INTERIOR CASING AND CONTROLLER OF 3M¿ RANGER¿ FLUID WARMING UNIT, MODEL 245 UPON OPENING THE UNIT FOR SERVICE BY THEIR TECHNICIAN. NO OTHER OBSERVATIONS WERE DISCOVERED WHILE IN USE. NO MEDICAL INTERVENTIONS WERE REQUIRED. NO PATIENT OR STAFF INJURY WAS ALLEGED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16396832 ↗MalfunctionFeb 13, 2023Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL REPORTED THAT UPON THE INITIAL INFUSION OF BLOOD VIA A 3M¿ RANGER¿ PRESSURE INFUSER, 14510 WITH THE USE OF 3M¿ RANGER¿ HIGH FLOW WARMING SET (MODEL 24355) LOT HX9090, BLOOD LEAKED AT THE LEUR CONNECTION. UPON TRANSFERRING THE PATIENT FROM THE OPERATING TABLE TO THE BED, THE COUPLING ALLEGEDLY BECAME LOOSE AND RELEASED QUICKLY RESULTING IN A LARGE OPENING IN THE LUMEN WITH BLOOD LEAKAGE. NO ISSUES OCCURRED WITH THE 3M¿ RANGER¿ PRESSURE INFUSER, AND NO PATIENT OR STAFF INJURY WAS ALLEGED. THE ADMINISTRATION OF FLUIDS WAS RESTARTED WITH A NEW CASSETTE. NO MEDICAL INTERVENTIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16362795 ↗MalfunctionFeb 13, 2023Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL REPORTED WHEN PURGING THE 3M¿ RANGER¿ HIGH FLOW WARMING SET (MODEL 24355) LOT HX9090 PIPELINE, THE COUPLING BECAME LOOSE, AND BLOOD LEAKED AT THE LEUR CONNECTION. NO PATIENT OR STAFF INJURY WAS ALLEGED. NO MEDICAL INTERVENTIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16362496 ↗MalfunctionFeb 2, 2023Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL ALLEGED 3M¿ RANGER¿ HIGH FLOW WARMING SET (MODEL 24355) LEAKED AT THE LEUR CONNECTION PROXIMAL TO THE PATIENT END WHILE PRIMING. NO PATIENT OR STAFF INJURY WAS ALLEGED. NO MEDICAL INTERVENTIONS WERE REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16283190 ↗MalfunctionFeb 1, 2023Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL ALLEGED 3M¿ RANGER¿ HIGH FLOW WARMING SET (MODEL 24355) LOT HX9181 LEAKED.. NO PATIENT OR STAFF INJURY WAS ALLEGED. NO MEDICAL INTERVENTIONS WERE REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16276844 ↗MalfunctionJan 18, 2023Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL ALLEGED 3M¿ RANGER¿ HIGH FLOW WARMING SET (MODEL 24355) LOT HX8986 LEAKED AT THE DRIP CHAMBER. NO PATIENT OR STAFF INJURY WAS ALLEGED. NO MEDICAL INTERVENTIONS WERE REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16196494 ↗MalfunctionJan 17, 2023Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL ALLEGED 3M¿ RANGER¿ HIGH FLOW WARMING SET (MODEL 24355) LOT HX8986 LEAKED AT THE DRIP CHAMBER. NO PATIENT OR STAFF INJURY WAS ALLEGED. NO MEDICAL INTERVENTIONS WERE REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16185545 ↗MalfunctionJan 16, 2023Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL ALLEGED 3M¿ RANGER¿ HIGH FLOW WARMING SET (MODEL 24355) LEAKED AT THE DRIP CHAMBER WHILE PRIMING WITH LACTATED RINGERS. DEVICE WAS NOT CONNECTED TO A PATIENT. NO PATIENT OR STAFF INJURY WAS ALLEGED. NO MEDICAL INTERVENTIONS WERE REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16180005 ↗MalfunctionJan 16, 2023Fluid/Blood Leak; Fluid/Blood Leak
A HOSPITAL ALLEGED THE INLET LINE CAME OUT OF THE SECOND RINGER'S LACTATE BAG AFTER USE OF 3M¿ RANGER¿ HIGH FLOW WARMING SET (MODEL 24355). NO PATIENT OR STAFF INJURY WAS ALLEGED. NO MEDICAL INTERVENTIONS WERE REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16179935 ↗
Other 3m Company products
- Steri-Drape11 models · 7 reports · 8 recalls
- 3M Attest5 models · 1 reports · 4 recalls
- 3M Steri-Drape4 models · 0 reports · 4 recalls
- 3M Ranger3 models · 73 reports · 1 recall
- Attest2 models · 0 reports · 2 recalls
- 3M Red Dot8 models · 16 reports · 1 recall
- Fast Release Varnish2 models · 2 reports · 1 recall
- Comply3 models · 1 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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