3M RangerRecalls & reported problems across all models
3m Company · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one 3M Ranger model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 73
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 3 models of 3M Ranger by 3m Company in the FDA's device registry (GUDID). Together they are named in 73 adverse event reports in the FDA's MAUDE database, received between Feb 23, 2023 and Jun 2, 2026 — classified as 73 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (65 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
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
3M Ranger recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Apr 22, 2025Open, Classified
Notice was issued to clarify flow rates related to the inlet fluid temperature.
Z-2231-2025 · Root cause: Device Design · Recall details · FDA record ↗
Most reported 3M Ranger problems
Device problems
- Fluid/Blood Leak65
- Leak/Splash6
- Improper or Incorrect Procedure or Method2
- Detachment of Device or Device Component1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions73
3M Ranger models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- 3M™ Ranger™ 24355Warmer, blood, non-electromagnetic radiation64 reports
- 3M™ Ranger™ 24750Warmer, thermal, infusion fluid1 recall0 reports
- 3M™ Ranger™ 24370Warmer, blood, non-electromagnetic radiation9 reports
Recent 3M Ranger adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJun 2, 2026Fluid/Blood Leak
A USER FACILITY REPORTED THAT THE SPIKES ON 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SETS APPEARED LOOSER THAN EXPECTED AND WERE PRONE TO SNAPPING WHEN INSERTED INTO BLOOD BAGS. THE SPIKE DETACHED FROM THE TUBING DURING USE. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25366312 ↗MalfunctionMay 14, 2026Fluid/Blood Leak
A USER FACILITY REPORTED THE TUBING ON A 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET SEPARATED FROM THE SPIKE DURING RAPID INFUSION. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25175164 ↗MalfunctionApr 7, 2026Fluid/Blood Leak
IT WAS REPORTED THE SPIKE ON TWO 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SETS DETACHED FROM THE TUBING WHEN THEY WERE CHANGING UNITS DURING A MASSIVE TRANSFUSION PROTOCOL. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTIONS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24811223 ↗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 ↗MalfunctionMar 26, 2026Detachment of Device or Device Component
A USER FACILITY REPORTED TWO 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SETS WERE INEFFECTIVE IN TRANSFUSING BLOOD PRODUCTS AS THEY WERE COMPROMISED DURING INFUSION. THE FIRST SET ALLEGED THAT THE SPIKE PORT WAS TWISTED CAUSING AN OCCLUSION. UPON CORRECTING IT, THE SPIKE SEPARATED FROM THE TUBING. ADDITIONALLY, THE SPIKE SEPARATED FROM THE TUBING ON A SECOND SET WHEN ATTEMPTING TO REMOVE IT FROM THE BLOOD BAG. THE CUSTOMER LATER REPORTED THE SETS DID NOT LEAK BUT WOULD HAVE DUE TO THE SPIKES DISCONNECTING FROM THE TUBING. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24700448 ↗MalfunctionMar 18, 2026Fluid/Blood Leak
A USER FACILITY REPORTED A 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET LEAKED AT THE Y CONNECTION WHEN BLOOD WAS BEING ADMINISTERED UNDER PRESSURE. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24627426 ↗MalfunctionMar 6, 2026Fluid/Blood Leak
IT WAS REPORTED THE SPIKE ON APPROXIMATELY FIVE 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SETS DETACHED FROM THE TUBING DURING RAPID TRANSFUSION OF BLOOD AND FLUIDS. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTIONS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24536275 ↗MalfunctionMar 3, 2026Fluid/Blood Leak
IT WAS REPORTED 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SETS LEAKED BLOOD WHEN THE CONNECTOR BROKE DURING INFUSION. THIS OCCURRED TWO DAYS IN A ROW. NO INJURIES OR MEDICAL INTERVENTIONS WERE REPORTED DUE TO THE ALLEGED MALFUNCTIONS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24500687 ↗MalfunctionFeb 11, 2026Fluid/Blood Leak
IT WAS REPORTED AFTER SETTING UP THE WARMER, FLUID LEAKAGE WAS OBSERVED FROM THE 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET. NO INJURIES OR MEDICAL INTERVENTIONS WERE REPORTED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24317190 ↗MalfunctionFeb 11, 2026Fluid/Blood Leak
A USER FACILITY REPORTED THE TUBING ON TWO 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SETS DISLODGED AT THE BASE ON THE SPIKE. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTIONS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24316628 ↗MalfunctionFeb 11, 2026Fluid/Blood Leak
A USER FACILITY REPORTED A 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET LEAKED AT THE CASSETTE WHEN CHANGING THE BLOOD BAG. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24316100 ↗MalfunctionDec 16, 2025Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THE 3M¿ RANGER¿ BLOOD/FLUID WARMING HIGH FLOW SET SPIKE DISLODGED WHEN ADMINISTERING BLOOD PRODUCTS. NO INJURIES OR MEDICAL INTERVENTIONS WERE REQUIRED DUE TO THE ALLEGED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23822515 ↗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 ↗
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
- Ranger10 models · 176 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page