Braun BNT300USRecalls & reported problems
Kaz USA, Inc. · Touch + No Touch Thermometer · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00328785003925), received between Nov 7, 2025 and Nov 7, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “False Negative Result” (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
- False Negative Result1
Patient problems
- Convulsion/Seizure1
- Fever1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 7, 2025False Negative Result; False Negative Result
A CONSUMER REPORTED THAT THEIR THERMOMETER HAD ALLEGEDLY PROVIDED A FALSE NEGATIVE READING ON THEIR GRANDDAUGHTER, WHO HAS A HISTORY OF FEBRILE SEIZURES. THE DEVICE ALLEGEDLY DISPLAYED A TEMPERATURE OF 100°F, AND THE CHILD SUBSEQUENTLY EXPERIENCED A FEBRILE SEIZURE. THE CHILD WAS TAKEN TO THE EMERGENCY ROOM, WHERE A HIGH FEVER WAS ALLEGEDLY CONFIRMED. NO ADDITIONAL MEDICAL DETAILS OR PATIENT OUTCOME WERE PROVIDED.
Patient problems: Convulsion/Seizure; Fever
MAUDE report 23503995 ↗
Other Thermometer, Electronic, Clinical devices
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- Welch Allyn, Inc. 901054Welch Allyn, Inc. · Thermometer, electronic, clinical2 recalls13 reports
- NA B105 VSP3.0 Patient MonitorGE Medical Systems Information Technologies, Inc. · Thermometer, electronic, clinical2 recalls0 reports
- Medline MDSTH1002Medline Industries, Inc. · Thermometer, electronic, clinical65 reports
- Mon-a-Therm 90050Covidien LP · Thermometer, electronic, clinical1 recall3 reports
- Mon-a-Therm 90044Covidien LP · Thermometer, electronic, clinical1 recall2 reports
- 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.