Red Dot™ 2239Recalls & reported problems
3m Company · 3M™ Red Dot™ Monitoring Electrodes with 3M™ Micropore™ Tape Backing, 50/Bag, 20/Case, 66 Plt 2239 · 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 10707387104426), received between Jun 21, 2019 and Jun 21, 2019 — 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
- Erythema1
- Itching Sensation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 21, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A DISTRIBUTOR REPORTED THAT A NURSE ALLEGED THAT A PATIENT EXPERIENCED ITCHINESS OF THE SKIN DURING MONITORING WITH TWELVE 2239 3M¿ RED DOT¿ ELECTRODES WITH 3M¿ MICROPORE¿ TAPE BACKING APPLIED ON THE CHEST FOR 24 HOURS OF HOLTER MONITORING IN A CEREBROVASCULAR CENTER. REDNESS OF THE SKIN WAS ALLEGED WHEN THE ELECTRODES WERE REMOVED THE NEXT DAY. THE ELECTRODES WERE NOT REAPPLIED AFTER THE SKIN SYMPTOMS OCCURRED. PHENIRAMINE WAS PRESCRIBED THE MORNING AFTER ELECTRODE REMOVAL. A DERMATOLOGIST EXAMINED THE PATIENT AND PRESCRIBED L-TRIAZINE (5MG, #1, ORALLY) AND ELOCOM CREAM, 15G FOR CONTACT DERMATITIS.
Patient problems: Erythema; Itching Sensation
MAUDE report 8724368 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.