ReliOn® Confirm Blue Blood Glucose Monitoring System 712002Recalls & reported problems
Wal-Mart Stores, Inc. · Portable 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00605388860163), received between Jan 23, 2018 and Jan 23, 2018 — 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.
Most reported problems
Device problems
- High Readings1
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.
InjuryJan 23, 2018High Readings; High Readings
CALLER STATED HE IS RECEIVING VERY HIGH READINGS. CUSTOMER STATED THE FIRST COUPLE WEEKS THE RESULTS WERE NORMAL. THE PAST WEEK AND A HALF HE HAS BEEN RECEIVING HIGH READINGS IN THE 240-320 RANGE. CALLER STATED HE MIS-DOSED DUE TO A METER RESULT OF 392 ON (B)(6) 2017 AT 1:32 PM. BECAUSE OF THE READING, HE TOOK HIS RAPID ACTING INSULIN (HUMALOG) AND HIS LONG-LASTING INSULIN (LANTUS). HE STARTED HAVING SYMPTOMS RIGHT AWAY. THE AMBULANCE/PARAMEDICS WERE CALLED AND THEY ARRIVED AROUND 2:00 PM, WHERE THEY ADMINISTERED A GLUCOSE PUSH AND TRANSPORTED HIM TO THE ER WHERE THEY ADMINISTERED A GLUCOSE DRIP. ONCE TREATMENT WAS COMPLETED, CALL WAS RELEASED. CALLER BELIEVES THE READING IN QUESTION WAS INACCURATE. CUSTOMER ONLY HAS ONE TEST STRIP LEFT FROM THIS LOT OF STRIPS. I ASKED HIM TO SEND IT BACK TO US. CALLER IS INSULIN DEPENDENT. CALLER IS ON OXYGEN THERAPY. CALLER IS ON NUMEROUS MEDICATIONS DUE TO MULTIPLE HEALTH ISSUES. CALLER'S TESTING TECHNIQUE IS CORRECT. CONTROLS WERE USED AND RESULTS WERE WITHIN RANGE.
Patient problems: Hypoglycemia
MAUDE report 7213493 ↗
Other SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER devices
- OneTouch Verio Flex 023-271LifeScan Europe GmbH · SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER3,703 reports
- FreeStyle Libre 2 71953Abbott Diabetes Care Inc · System, test, blood glucose, over the counter2 recalls1 death3,286 reports
- OneTouch Ultra2 021-105LifeScan U.S. LLC · SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER1,731 reports
- Omnipod DASH PDM PDM-USA1-D001-MG-USA1Insulet Corporation · System, Test, Blood Glucose, Over The Counter1 recall10 deaths1,129 reports
- Omnipod UST400Insulet Corporation · System, Test, Blood Glucose, Over The Counter12 deaths816 reports
- TRUE METRIX TRUE METRIX SELF MONITORING BLOOD GLUCOSE METER - NOT FOR RETAIL SALETrividia Health, Inc. · System, Test, Blood Glucose, Over The Counter418 reports
- FreeStyle Freedom Lite 70923-70Abbott Diabetes Care Inc · SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER378 reports
- FreeStyle Lite 70829-70Abbott Diabetes Care Inc · SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER378 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page