Red Dot™ 2268-3Recalls & reported problems
3m Company · 2268-3 RED DOT SOFT CLOTH MON ELECTRODE 3/BAG, 200 BAGS/CASE · Class 2
- 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 10707387770676), received between Sep 27, 2022 and Sep 27, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component1
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.
MalfunctionSep 27, 2022Detachment of Device or Device Component
BEDSIDE RN REMOVED EKG LEADS FROM PATIENT, THE STICKER ITSELF CAME OFF HOWEVER THE STICKY ADHESIVE REMAINED ON PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15492305 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.