Medline MPH4550Recalls & reported problems
Medline Industries, Inc. · STRIP,GLUCOSE,EVENCARE PRO · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277409170), received between Nov 1, 2022 and Sep 24, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Low 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Low Readings1
Patient problems
- Hypoglycemia1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Low Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50885795 ↗InjuryNov 1, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY ON (B)(6) 2022 A RESIDENTS BLOOD SUGAR WAS BEING CHECKED PER POLICY AND PROTOCOL AND THE STAFF MEMBER NOTED, 'THE NUMBER APPEARED HIGHER THAN USUAL'. THE STAFF MEMBER RECHECKED THE BLOOD SUGAR AND STILL RECEIVED A 'HIGH NUMBER' AND GAVE THE RESIDENT SLIDING SCALE INSULIN.
Patient problems: Hypoglycemia
MAUDE report 15710052 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.