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Kendall 33110RRecalls & reported problems

Cardinal Health, Inc. · DL Disposable Cable and Lead Wire System 10 Lead, Adapter Required · Class 2

All models of Kendall (35)

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

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 10884521516359), received between Apr 21, 2021 and Apr 21, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Read Input Signal” (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

  • Failure to Read Input Signal1
  • Illegible Information1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionApr 21, 2021Failure to Read Input Signal; Illegible Information; Failure to Read Input Signal; Illegible Information

    CUSTOMER REPORTS: WHEN THE CUSTOMER USED THE CABLES TO PERFORM AN ECG THERE ARE SOME ARTIFACTS AND THE RESULT IS NOT LEGIBLE. TWO CABLES FROM THE SAME LOT WERE USED IN THE SAME PATIENT WITH THIS PROBLEM. NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11700972 ↗

Other CABLE, ELECTRODE devices

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Sources and updates

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