Kendall 33561Recalls & reported problems
Cardinal Health 200, LLC · Kendall DL Adapter, 10 Lead, For Philips Intellivue Monitors, Reusable, Non-sterile · Class 2
All models of Kendall (31)
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 20885380189262), received between Aug 11, 2025 and Aug 11, 2025 — 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.
Reports received per month
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings1
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.
MalfunctionAug 11, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
THE CUSTOMER REPORTED AN ALARMING PHILIPS BEDSIDE MONITOR. THE BEDSIDE MONITOR WAS DISPLAYING ONLY LEAD II AND WAS CONTINUOUSLY ALARMING WITH "ECG CHECK CABLE". IT ALSO SHOWED THAT THE PATIENT'S ECG LEAD II WAS THE ONLY LEAD THAT THE MONITOR WAS READING. ALSO, THE ECG WAVEFORM LOOKED UPSIDE DOWN AND THE PHILIPS SOFTWARE WAS READING THE RHYTHM AS "SV RHYTHM". THE CUSTOMER DISCOVERED THAT THE ECG TRUNK CABLE HAD BEEN INSERTED INCORRECTLY INTO THE MODULE/ADAPTER. ADDITIONAL INFORMATION RECEIVED ON 24JUL2025 STATED THAT THE CARDINAL ECG LEADWIRES WERE ABLE TO BE PLACED IN THE ECG ADAPTER INVERTED. THIS ALLOWS THE MONITOR TO SEE THAT THE LEADWIRES ARE PLUGGED IN BUT DISPLAYS AN INCORRECT ECG SIGNAL. ONCE THEY FLIPPED THE CABLE (INVERTED IT CORRECTLY), THE ECG STARTED READING CORRECTLY. PHOTO AND VIDEO PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22772970 ↗
Other CABLE, ELECTRODE devices
- N/A ECG Leadwire set, 5-lead, grouped, grabber, AHA, mix 74 cm/ 29 in, 130 cm/ 51 inGE Healthcare Finland Oy · CABLE, ELECTRODE1 recall1 report
- N/A ECG Leadwire set, 5-lead, snap, AHA, 74 cm/ 29 inGE Healthcare Finland Oy · CABLE, ELECTRODE1 recall0 reports
- N/A ECG Leadwire set, 5-lead V2-6, snap, AHA, 74 cm/ 29 inGE Healthcare Finland Oy · CABLE, ELECTRODE1 recall0 reports
- N/A ECG Leadwire set, 3-lead, snap, AHA, 74 cm/ 29 inGE Healthcare Finland Oy · CABLE, ELECTRODE1 recall0 reports
- N/A ECG Leadwire set, 5-lead, snap, AHA, 130 cm/ 51 inGE Healthcare Finland Oy · CABLE, ELECTRODE1 recall0 reports
- N/A ECG TRUNK CABLE, 12-LEAD, AHA, 1.2 M/4 FTGE Healthcare Finland Oy · CABLE, ELECTRODE1 recall0 reports
- N/A ECG Leadwire set, 5-lead, snap, AHA, mix 74 cm/ 29 in, 130 cm/ 51 inGE Healthcare Finland Oy · CABLE, ELECTRODE1 recall0 reports
- N/A ECG TRUNK CABLE, 3-LD W/ INTEGRATED GRABBER LEAD WIRE, AHA, 3.6 M/12 FTGE Healthcare Finland Oy · CABLE, ELECTRODE1 recall0 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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