Meijer Essential Blood Glucose Meter 8000-07081Recalls & reported problems
Meijer, Inc. · Blood Glucose Meter, Meijer, Essential · 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 10760236150357), received between Jan 16, 2025 and Jan 16, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Hypoglycemia1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 16, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
CALLER SAYS THE PATIENT'S MEIJER ESSENTIAL BLOOD GLUCOSE METER, WHICH WAS RECENTLY PURCHASED WAS READING 170 MG/DL/180 MG/DL. THEN STARTED PATIENT STARTED FEELING ILL (TIME FROM MEASUREMENT TO ONSET OF SYMPTOMS UNKNOWN) AND AN AMBULANCE WAS CALLED. EMTS MEASURED BLOOD GLUCOSE (BGM BRAND NOT REPORTED OR TIME BETWEEN THIS MEASUREMENT AND THOSE WITH THE MEIJER ESSENTIAL IS NOT KNOWN), 34 MG/DL. PATIENT HAS BEEN IN THE HOSPITAL FOR 4 DAYS. THE REPORTER WENT TO MEIJER BUT THE PHARMACIST COULD NOT HELP AND SUGGESTED TO CONTACT AGAMATRIX CUSTOMER SERVICE. THE CALLER WAS FRUSTRATED BECAUSE THE PHARMACIST SHOWED NO COMPASSION OR EMPATHY, FELT LIKE HE WAS DISMISSED.
Patient problems: Hypoglycemia
MAUDE report 21167318 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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