Red Dot™ 2330Recalls & reported problems
3m Company · 2330 RESTING EKG ELECT 10EA/CD · Class 2
All models of Red Dot (14)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 10707387195455), received between Sep 9, 2024 and Sep 9, 2024 — classified as 1 malfunction.
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Patient problems
- Chest Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 9, 2024
PATIENT WITH ACTIVE CHEST PAIN. PROCEDURE ELECTROCARDIOGRAM (EKG). THE EKG ELECTRODES WOULD NOT ADHERE TO PATIENT SKIN. THE ONES THAT DID STICK, WERE NOT CONDUCTING WELL. THIS TOOK ALMOST 15 MINUTES TO GET AN ADEQUATE EKG, DELAY IN PROCEDURE. NO KNOWN HARM TO PATIENT.
Patient problems: Chest Pain
MAUDE report 20168414 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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