Medi-Trace Cadence 22550PC (UDI 20192253017578)Recalls & reported problems
Cardinal Health 200, LLC · Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes, Pre-Connect · Class 3
All models of Medi-Trace Cadence (5)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20192253017578), received between Oct 4, 2022 and Oct 4, 2022 — classified as 1 death.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (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
Device problems
- Loss of or Failure to Bond1
Patient problems
- Asystole1
- Heart Failure/Congestive Heart Failure1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
DeathOct 4, 2022Loss of or Failure to Bond; Loss of or Failure to Bond
CUSTOMER REPORTS: FOUR DEFIB PADS WERE OPENED FOR USE DURING A RESUSCITATION SITUATION AND AN ATTEMPT WAS MADE TO STICK THEM TO THE PATIENT, BUT THEY DID NOT STICK AND SLIPPED OFF THE PATIENT'S CHEST. RHYTHM CONTROL AND DEFIBRILLATION WERE NOT POSSIBLE AT THAT TIME. PER ADDITIONAL INFORMATION RECEIVED ON 10/04/2022, THE PATIENT DIED.
Patient problems: Asystole; Heart Failure/Congestive Heart Failure
MAUDE report 15538912 ↗
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- 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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