ReliOn™ Premier Compact Blood Glucose Monitoring System 783110Recalls & reported problems
Wal-Mart Stores, Inc. · The ReliOn Premier Compact Blood Glucose Monitoring System is intended for the quantitative measurement of glucose in fresh capillary whole blood samples drawn from the fingertips and alternative sites such as the forearm, palm, thigh and calf. Carton contains: ReliOn Premier Compact Meter DI# 30681131240728, ReliOn Premier Test Strips 50ct DI# 00681131169776, Lancing Device, Lancets and Literature. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00681131240727), received between Nov 27, 2024 and Nov 27, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “High Readings” (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
- High Readings1
Patient problems
- Ambulation or Postural Difficulties1
- Dizziness1
- Hypoglycemia1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 27, 2024High Readings; High Readings
THE PATIENT HAD LUNCH AT ABOUT 12:00 PM. THE CALLER STATED THAT SHE TESTED HER NEPHEW ABOUT TWO HOURS LATER AND RECEIVED A READING OF 400 WITH THIS METER, AND THEN RECEIVED ANOTHER READING OF WHAT SHE THINKS WAS 600 WITH THIS METER. THE CALLER TREATED THE PATIENT BASED ON THESE READINGS WITH NOVOLOG WHICH IS HIS FAST-ACTING INSULIN. SHE USED THE SAME BLOOD DROP FOR ALL TESTS. AFTER ABOUT 45 MINUTES, THE PATIENT THEN STARTED DISPLAYING SYMPTOMS, SUCH AS HE COULD NOT WALK AND WAS LIGHTHEADED AND DIZZY. THE CALLER DID NOT TAKE THE PATIENT TO THE ER OR CALL THE PARAMEDICS AND JUST TREATED HIM AT HOME. SHE GAVE HIM SOME ORANGE JUICE, GLUCOSE TABLETS, AND A COKE TO BRING HIS BLOOD SUGAR BACK UP. THE CALLER WOULD LIKE TO SWITCH TO THE CLASSIC METER BECAUSE IT HAS A MEMORY AND DATE/TIME STAMP FOR THE RESULTS. REPLACED METER, STRIPS AND SENT RETURN LABEL.
Patient problems: Ambulation or Postural Difficulties; Dizziness; Hypoglycemia
MAUDE report 20794703 ↗
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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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