Kendall 31424743Recalls & reported problems
Cardinal Health 200, LLC · KittyCat 1051NPSM Neonatal, Radiolucent, Monitoring Cloth electrode ( 3/PK) · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20192253017356), received between Oct 12, 2023 and Oct 12, 2023 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE CUSTOMER REPORTED THAT A BURN OCCURRED ON ONE OF THEIR MICRO PREEMIES. THE LEADS THEY USE ARE CARDINAL HEALTH KENDALL 1051NPSM NEONATAL ELECTRODES. THEY ARE PRE-WIRED, SMALL CLOTH AND RADIOLUCENT. THE BABY HAS HEALED BUT SEEMS TO HAVE A MARK NOW. THE PATIENT WAS PRESCRIBED BACTROBAN.
Patient problems: Burn(s)
MAUDE report 17924898 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.