Ten20 Conductive Paste 10-20-8Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00891893002239), received between Jan 21, 2021 and Dec 16, 2022 — classified as 2 injuries.

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryDec 16, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ON (B)(6) 2022 A 60 YEAR OLD FEMALE PATIENT AT MUSC HAD AN OVERNIGHT SLEEP STUDY CONDUCTED. TEN20 PASTE WAS USED FOR MONITORING LEADS DURING THE STUDY. THE STUDY WAS COMPLETED PER PROCEDURE WITHOUT ISSUE AND THE PATIENT WAS SENT HOME. UPON RETURN HOME, WHILE WASHING THE PRODUCT FROM HAIR, THE PATIENT STATED THE PRODUCT RAN INTO HER EYES RESULTING IN CORNEAL SCRATCHING REQUIRING TREATMENT BY AN EYE DOCTOR.

  Patient problems: Eye Pain

  MAUDE report 16000270 ↗
• InjuryJan 21, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  EMPLOYEE FROM SLEEP CENTER CALLED REGARDING A PATIENT OF THEIRS RINSING TEN20 CONDUCTIVE PASTE OUT OF HAIR AND IT GOT IN THE PATIENT'S EYE, CAUSING IRRITATION. SLEEP CENTER EMPLOYEE STATED THAT THEIR PATIENT HAS MADE AN APPOINTMENT WITH THEIR PHYSICIAN.

  Patient problems: Eye Pain

  MAUDE report 11208390 ↗