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3M™ 2228Recalls & reported problems

3m Company · ECONOMY ELECTRODE FOAM IN-PROCESS, 2228 FOAM MONITORING ELECTRODE , 50/BAG, 20/CASE, 72/PLT · Class 2

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier.

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.

Recalls naming this device

  1. Sep 15, 2020Terminated

    Corrosion could cause performance failures in the product.

    Z-0421-2021 · Root cause: Process control · FDA record ↗

  2. Sep 15, 2020Terminated

    Corrosion could cause performance failures in the product.

    Z-0422-2021 · Root cause: Process control · FDA record ↗

Other Electrode, electrocardiograph devices

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