Medline MDS9950BRecalls & reported problems
Medline Industries, Inc. · THERMOMETER,DIGI,ORAL,PREMIER,F/C,30 SEC · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00888277115630), received between Dec 11, 2023 and Sep 28, 2026 — classified as 3 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Computer Software Problem1
- Incorrect, Inadequate or Imprecise Result or Readings1
- Output Problem1
- Unexpected Shutdown1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916296 ↗MalfunctionSep 21, 2026Computer Software Problem; Unexpected Shutdown
It was reported that "They have been shutting down prior to measuring the temperature."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50841502 ↗MalfunctionDec 11, 2023Output Problem; Output Problem
"THE READINGS ARE CONSISTENTLY READING LOW BY AS MUCH AS 1*F".
Patient problems: Insufficient Information
MAUDE report 18300875 ↗
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- Temperature Probes Esophageal/Rectal Temperature ProbePhilips Medical Systems Hsg · Thermometer, electronic, clinical1 recall1 report
- CARESCAPE B450 MBA313GE Healthcare Finland Oy · Thermometer, electronic, clinical1 recall1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.