Kendall 22855 (REF 22855-)Recalls & reported problems
Cardinal Health 200, LLC · Kendall 855 FOAM ELECTRODES, Conductive Adhesive Hydrogel, Radiolucent · 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 20192253016755), received between Aug 25, 2025 and Aug 25, 2025 — 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
- Fluid Discharge1
- Full thickness (Third Degree) Burn1
- Necrosis1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE CUSTOMER REPORTED THAT THEY HAD AN INCIDENT WITH ELECTRODE 22855 AND A PATIENT WAS HARMED IN THE MRI. ON 19AUG2025 ADDITIONAL INFORMATION WAS RECEIVED STATING THAT THE PATIENT HAD AN MRCP ORDERED AND AFTER THE EXAM, WHICH LASTED ABOUT 15 MINUTES, THE PATIENT COMPLAINED OF WARMTH TO THE UPPER LEFT CHEST. IT WAS DETERMINED THAT ONE OF THE FOAM ELECTRODES ON THE UPPER LEFT CHEST HAD BEEN LEFT DURING THE EXAM. THE PATIENT HAD BEEN SCANNED FOR METAL, BUT THIS ELECTRODE DOES NOT SCAN. THE TECH LOOKED UNDER THE ELECTRODE IMMEDIATELY AFTER THE SCAN AND ONLY SAW SLIGHT REDNESS. THE PATIENT HAS BEEN SEEN AT THE WOUND CARE CENTER FOR TREATMENT OF THE BURN. THE WOUND HAS BEEN CLASSIFIED AS A 3RD DEGREE BURN. IT WAS STATED THAT THE INSTRUCTIONS FOR USE WERE FOLLOWED. ON 21AUG2025 ADDITIONAL INFORMATION WAS RECEIVED STATING THAT 8 DAYS AFTER THE EVENT THE PATIENT WAS SEEN AT THE WOUND CARE CENTER (B)(6) 2025). THE PHYSICIAN DOCUMENTED A L ANTERIOR CHEST WALL 3RD DEGREE, FULL THICKNESS THERMAL BURN. THE WOUND WAS DEBRIDED, SILVADENE WAS CONTINUED. THE PATIENT WAS SEEN AGAIN ON (B)(6) 2025, THE WOUND IS CLASSIFIED AS FULL THICKNESS AND MEASURES 3.9CM LENGTH, 2.6CM WIDTH, 0.3CM DEPTH, 7.964CM/2
Patient problems: Fluid Discharge; Full thickness (Third Degree) Burn; Necrosis
MAUDE report 22890258 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.