Medline MPH1550Recalls & reported problems
Medline Industries, Inc. · STRIP,EVENCARE G2,600 EA/CS,50 EA/BX · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00884389102568), received between May 22, 2026 and Sep 30, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (3 reports).
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
- Incorrect, Inadequate or Imprecise Result or Readings3
- Unable to Obtain Readings2
- Failure to Obtain Sample1
- Failure to Read Input Signal1
- Overheating of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Unable to Obtain Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952346 ↗MalfunctionSep 29, 2026Failure to Read Input Signal
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934840 ↗MalfunctionSep 25, 2026Incorrect, Inadequate or Imprecise Result or Readings
It was reported that his test strips were reading out of range after testing them and the meter against the control solutions. His other bottle still read out of range.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50902690 ↗MalfunctionSep 22, 2026Unable to Obtain Readings; Failure to Obtain Sample
It was reported that THEY KEEPS GETTING ERROR THAT THERE IS NOT ENOUGH BLOOD TO READ. TEST STRIPS ARE NOT PULLING IT IN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50856364 ↗MalfunctionSep 21, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50841878 ↗MalfunctionMay 22, 2026Overheating of Device; Incorrect, Inadequate or Imprecise Result or Readings
PER THE REPORT, "CUSTOMER CALLED IN STATING HER GLUCOSE MONITOR IS NOT WORKING PROPERLY. SHE ALSO STATED SHE THINKS HER STRIPS ARE NOT WORKING AS THEY SHOULD. SHE MENTIONED STRIPS WERE EXPOSED TO HEAT AND MAY HAVE BEEN DAMAGED AND MAY BE CAUSING HER GLUCOSE READINGS TO BE OFF. REQUESTED REPLACEMENT STRIPS ASAP."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25262717 ↗
Other SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER devices
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- 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
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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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