Skip to content

Medi-Trace Cadence 22550A (REF 22550A-)Recalls & reported problems

Cardinal Health 200, LLC · Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes · Class 3

All models of Medi-Trace Cadence (5)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20192253017547), received between Sep 26, 2023 and Apr 23, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Connection 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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 1 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Connection Problem1
  • Temperature Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • Superficial (First Degree) Burn1

Recent adverse event reports

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

  • MalfunctionApr 23, 2024Connection Problem; Connection Problem

    THE CUSTOMER REPORTED THAT WHEN USING THE DEVICE, THE PLATE CONNECTOR WAS NOT ATTACHED TO THE DEFIBRILLATOR. THE CONNECTOR APPEARED BENT AND THAT PREVENTED IT FROM CONNECTING. THE CUSTOMER FURTHER STATED THAT THE DEVICE HAD BEEN STORED PROPERLY AND THE PACKAGING WAS OPENED AT THE TIME OF USE. THERE WAS NO HARM TO THE PATIENT INVOLVED. ADDITIONAL INFORMATION WAS RECEIVED FROM THE CUSTOMER AND STATED THAT THE PART INVOLVED IN THE ISSUE WAS A BEND IN THE FIRST METAL PIN, THE ONE NEAR THE FIXING TAB (THE FIRST FROM THE TOP) INSIDE ITS PROTECTIVE PART, WHICH WAS NEITHER CRUSHED NOR DAMAGED. IT WAS FOLDED AND RESTING AGAINST THE WALL OF THE PROTECTION AND PREVENTED IT FROM FITTING ONTO THE CABLE SOCKET.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19163224 ↗
  • MalfunctionSep 26, 2023Temperature Problem; Temperature Problem

    THE CUSTOMER REPORTED DURING A DIRECT CURRENT CARDIOVERSION TO TREAT AN ATRIAL FLUTTER THERE WAS A SPARK ON THE ANTERIOR LEFT CHEST PAD. THE PATIENT CONVERTED TO SINUS RHYTHM AFTER 1 SHOCK AT 250 JOULES AND THE PAD WAS REMOVED FROM THE PATIENT'S CHEST. TWO THERMAL BURNS APPROXIMATELY 1/2"X2" WERE FOUND. THE PATIENT RECEIVED SUPERFICIAL (FIRST DEGREE) BURNS.

    Patient problems: Superficial (First Degree) Burn

    MAUDE report 17816895 ↗

Other Automated external defibrillators (non-wearable) devices

All Automated external defibrillators (non-wearable) devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page