Medline MPHUA120MRecalls & reported problems
Medline Industries, Inc. · ANALYZER,URINE,MEDLINE 120 MINI · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277720336), received between Aug 31, 2026 and Sep 8, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Computer Software Problem” (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
- Computer Software Problem1
- Incorrect, Inadequate or Imprecise Result or Readings1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2026Computer Software Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676544 ↗MalfunctionAug 31, 2026Incorrect, Inadequate or Imprecise Result or Readings
It was reported that "THE RESULTS ON THE STRIP ARE NOT COINCIDING WITH THE ANALYZER REPORT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50518843 ↗
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- Albustix® Reagent Strips 10333485Siemens Healthcare Diagnostics Inc. · METHOD, ENZYMATIC, GLUCOSE (URINARY, NON-QUANTITATIVE)1 report
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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