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Medi-Trace Cadence 22770PRecalls & reported problems

Cardinal Health, Inc. · Pediatric Multi-Function Defibrillation Electrodes,Radiotransparent, · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20884527022387), received between Mar 6, 2020 and Mar 6, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Sense” (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

Device problems

  • Failure to Sense1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionMar 6, 2020Failure to Sense; Failure to Sense

    THE CUSTOMER REPORTED THAT WHEN THE PATIENT IN FULL CARDIAC ARREST ARRIVED VIA EMS TO THE TRAUMA ROOM, PEDIATRIC ZOLL PADS WERE APPLIED AND THE RHYTHM WAS NOT SHOWING ON THE MONITOR DESPITE GOOD QUALITY COMPRESSIONS ONGOING. NEW PADS WERE APPLIED. IT WAS NOTED THAT THE 1ST SET OF PADS DID NOT HAVE GEL. ADDITIONAL INFORMATION WAS RECEIVED STATING THAT THERE WAS A MINIMUM INTERRUPTION AS PADS NEED TO BE CHANGED. THE PATIENT CURRENT STATUS IS UNKNOWN.

    Patient problems: No Information

    MAUDE report 9801279 ↗

Other PACEMAKER, CARDIAC, EXTERNAL TRANSCUTANEOUS (NON-INVASIVE) devices

All PACEMAKER, CARDIAC, EXTERNAL TRANSCUTANEOUS (NON-INVASIVE) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.