Medline MDSTS101Recalls & reported problems
Medline Industries, Inc. · THERM,STRIP,FOREHEAD,DISP, 5000 EA/CS · Class 2
- 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 10888277681958), received between Sep 21, 2026 and Sep 23, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Incorrect Measurement” (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
- Incorrect Measurement1
- 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 23, 2026Incorrect Measurement
It was reported that "The anesthesia provider stated the Medline product was off by a full degree, therefore are not accurate."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870299 ↗MalfunctionSep 21, 2026Incorrect, Inadequate or Imprecise Result or Readings
It was reported that they do not work.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50846314 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.