Kendall 31050522Recalls & reported problems
Cardinal Health, Inc. · 200 Foam Electrodes,Conductive Adhesive Hydrogel · 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 20884527007926), received between Nov 2, 2021 and Nov 2, 2021 — 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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Anaphylactic Shock1
- Asthma1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 2, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
CUSTOMER REPORT AN ALLERGIC REACTION TO ECG ELECTRODES THAT CAUSED AN ANAPHYLACTIC REACTION, ASTHMA ATTACK AND HIVES AFTER A SLEEP STUDY.
Patient problems: Anaphylactic Shock; Asthma
MAUDE report 12741189 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.