Ranger™ 24200 (UDI 50707387781397)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50707387781397), received between Apr 30, 2019 and Apr 30, 2019 — classified as 1 malfunction.

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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 30, 2019Fluid/Blood Leak; Fluid/Blood Leak

  A HOSPITAL ANESTHESIA TECHNICIAN REPORTED A (B)(6) MALE PATIENT, WEIGHING 20KG, HAD LIVER TRANSPLANT SURGERY ON (B)(6) 2019. THE PATIENT WAS BEING ADMINISTERED RBC FLUID THROUGH A 3M¿ RANGER¿ STANDARD FLOW DISPOSABLE SET (MODEL 24200) WARMED BY A 3M¿ RANGER¿ WARMING UNIT (MODEL NOT SPECIFIED). PRIOR TO ADMINISTRATION, THE FLUID WARMING CASSETTE WAS LOADED INTO THE WARMING UNIT. THE WARMING UNIT WAS TURNED OFF AT THIS TIME. THE PATIENT WAS ADMINISTERED RBC FLUID FOR APPROXIMATELY 2 TO 2 ½ HOURS. NO PRESSURE DEVICE OR PUMP WAS USED. NO MANUAL PRESSURE WAS APPLIED TO THE FLUID BAGS. THE EMPLOYEE ALLEGED, APPROXIMATELY 2 TO 2 ½ HOURS AFTER THE START OF ADMINISTRATION, THE ANESTHESIOLOGIST DISCOVERED BLOOD WAS LEAKING FROM THE RANGER ¿ UNIT. THE ANESTHESIOLOGIST TOOK ACTION TO PREVENT ANY BODILY HARM TO THE PATIENT. THE EMPLOYEE REPORTED THE WARMING UNIT WAS UNABLE TO BE EVALUATED AT THE HOSPITAL DUE TO BLOOD CONTAMINATION.

  Patient problems: Not Applicable

  MAUDE report 8564910 ↗