Kendall 33136TRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521212602), received between Nov 25, 2020 and Nov 25, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (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

Recent adverse event reports

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

• MalfunctionNov 25, 2020Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER REPORTED THAT CDH TELEMETRY IS HAVING CONSISTENT ISSUES WITH THE LEADS AND MX40 ADAPTERS CAUSING INCONSISTENT TRACINGS. THERE WAS NO PATIENT HARM. ADDITIONAL INFORMATION PROVIDED STATED THAT THE LEADS WERE PROVIDING INCONSISTENT READINGS, SHOWING "LEADS OFF", AND PROVIDING FALSE ALARMS. THERE WAS NO IMPACT TO THE PATIENT AS A RESULT OF THE INCONSISTENT READINGS. IT IS HARD FOR THE CUSTOMER TO PINPOINT EXACTLY WHAT THE ISSUE IS AS THEY SOMETIMES SWITCH THE ADAPTERS AND SOMETIMES SWITCH THE LEADS OUT. THE ISSUE IS NOT OCCURRING WITH EVERY LEAD SET. IT WAS NOTED THAT THE TELEMETRY BOXES SOMETIMES GO BAD WHERE THE ADAPTERS CONNECT SO THE PINS SOMETIMES DEGRADE. THE CUSTOMER FURTHER STATED THAT BY KEEPING THE ADAPTERS ATTACHED TO THE MONITORS, THEY THINK THEY ARE SEEING IMPROVED TRACINGS. IT IS UNKNOWN IF THE LEADS/ADAPTERS ARE CAUSING THE ISSUES.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10900257 ↗