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Dexcom Discovery Sensor 3 Pack STS-DE-003Recalls & reported problems

Dexcom, Inc. · G6 Discovery Sensor 3pk, US · Class 2

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

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

1 FDA recall record 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. Feb 3, 2020Terminated

    The company identified potential interference from hydroxyurea. Patient use of the anti-neoplastic drug may falsely elevate glucose readings on the Continuous Glucose Monitoring Systems.

    Z-1562-2020 · Root cause: Under Investigation by firm · FDA record ↗

Other Integrated Continuous Glucose Monitoring System, Factory Calibrated devices

All Integrated Continuous Glucose Monitoring System, Factory Calibrated devices →

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