S-SCORT® lll 74000Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI B245740000), received between Mar 6, 2018 and Dec 6, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Battery Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 6, 2024Fitting Problem; Fitting Problem

  REPORTED STATED THAT DEVICE MODEL 74000 FAILED TO SUCTION DURING AN ATTEMPT TO SUCTION A CARDIAC ARREST PATIENT. AFTER DEVICE CASE WAS OPENED IT WAS DETERMINED TAH FITTING THAT CONNECTS FROM PUMP TO ELBOW WAS BROKEN. NO ADDITIONAL INFORMATION WAS REQUIRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20868389 ↗
• MalfunctionMar 6, 2018Battery Problem; Battery Problem

  PER CUSTOMER (USER): "THE UNIT IN QUESTION WAS USED DURING CARDIAC ARREST AND FAILED WHEN SUCTION WAS ATTEMPTED. THE FAILURE DID NOT HAVE AN IMPACT ON THE OUTCOME OF THE PATIENT. THE UNIT WAS JUST PURCHASED A FEW MONTHS AGO AND WASN'T PLACED INTO SERVICE UNTIL THE MIDDLE OF (B)(6). THE UNIT SAT IN THE CLOSED BOX UNTIL THE AMBULANCE INSPECTION WITH THE STATE. I HAVE ALREADY PURCHASED A REPLACEMENT BATTERY AND THE UNIT IS ALREADY BACK IN SERVICE AND FUNCTIONING FINE. AT THIS TIME WE WILL NOT BE SUBMITTING ANY ADDITIONAL INFORMATION AS THE BATTERY FAILURE HAD NOTHING TO DO WITH THE PATIENTS OUTCOME."

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7318170 ↗