3M™ Red Dot™ 2660-3Recalls & reported problems
3m Company · 3M™ Red Dot™ ECG Monitoring Electrodes, 2660-3, Radiolucent, Soft Cloth · 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 10707387789098), received between May 23, 2023 and May 23, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Human-Device Interface Problem” (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
- Human-Device Interface Problem1
Patient problems
- Erythema1
- Skin Inflammation/ Irritation1
- Skin Tears1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 23, 2023Human-Device Interface Problem; Human-Device Interface Problem
REPORT RECEIVED VIA MEDWATCH 4900240000-2023-8070: A HOSPITAL REPORTED A FEMALE PATIENT ALLEGEDLY EXPERIENCED SKIN REMOVAL, IRRITATION WITH ERYTHEMA AND A RASH WITH THE USE OF THE 3M¿ RED DOT¿ ELECTRODE. NO MEDICAL INTERVENTION WAS REPORTED.
Patient problems: Erythema; Skin Inflammation/ Irritation; Skin Tears
MAUDE report 16988958 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.