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Advocate Redi-Code+ Speaking Blood Glucose Meter BMB-001SRecalls & reported problems

Diabetic Supply Of Suncoast, Inc. · Advocate Redi-Code+ Speaking Blood Glucose Meter · Class 2

Data updated Oct 18, 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 00894046001882), received between Aug 23, 2023 and Aug 23, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Power Up” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Failure to Power Up1

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.

  • MalfunctionAug 23, 2023Failure to Power Up; Failure to Power Up

    METER IS NOT WORKING EVEN AFTER REPLACING THE BATTERIES. CUSTOMER SAID SHE HAD IT IN THE LIVING ROOM THEN ALL OF A SUDDEN, WHEN SHE WAS ABOUT TO USE IT THE OTHER DAY, IT JUST WON'T WORK.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17601891 ↗

Other System, Test, Blood Glucose, Over The Counter devices

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Sources and updates

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