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3M™ Red Dot™ 2570-5Recalls & reported problems

3m Company · 3M™ Red Dot™ ECG Monitoring Electrodes, 2570-5, Radiolucent, Foam, Diaphoretic, with Abrader · 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 10707387789333), received between Sep 21, 2022 and Sep 21, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Signal Artifact/Noise” (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

  • Signal Artifact/Noise1

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 21, 2022Signal Artifact/Noise

    3M ECG PADS PHYSICALLY DRY, POOR SIGNAL CONDUCTION FOR ECG. PADS WERE REMOVED FROM A SEALED PACKAGE. DELAYED START TIME FOR CARDIOVASCULAR OPERATING ROOM. ACTUAL PADS NOT SAVED. PICTURE IS REPRESENTATION FOR THE PRODUCT, BOTH FROM THE SAME BOX WITH THE SAME LOT #. MANUFACTURER RESPONSE FOR ECG PAD, (BRAND NOT PROVIDED) (PER SITE REPORTER). WILL WATCH.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15461653 ↗

Other Electrode, electrocardiograph devices

All Electrode, electrocardiograph devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.