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
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 ↗
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- NA 861289Philips Medical Systems Hsg · Automated External Defibrillators (Non-Wearable)7 deaths3,385 reports
- R SERIES 30001005201310012Zoll Medical Corporation · Automated external defibrillators (non-wearable)10 deaths1,720 reports
- PHILIPS HeartStart FRxPhilips Electronics North America Corporation · Automated external defibrillators (non-wearable)26 deaths1,586 reports
- LIFEPAK CR2 99512Physio-Control, Inc. · Automated external defibrillators (non-wearable)8 deaths1,502 reports
- Lifeline Configuration DDU-100ADefibtech, L.L.C. · Automated External Defibrillators (Non-Wearable)1 death1,285 reports
- PHILIPS HeartStart FR3Philips Electronics North America Corporation · Automated External Defibrillators (Non-Wearable)10 deaths1,188 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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