Braun IRT6575USRecalls & reported problems
Kaz USA, Inc. · BRAUN THERMOSCAN 7 PLUS CONNECTED · 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 00328785007909), received between Aug 28, 2024 and Sep 24, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “False Negative Result” (3 reports).
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 Result3
Patient problems
- Fever3
- Convulsion/Seizure1
- Viral Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026False Negative Result
Patient problems: Fever
MAUDE report 50888896 ↗MalfunctionApr 17, 2026False Negative Result
A CONSUMER REPORTED THAT THEIR THERMOMETER (IRT6575) ALLEGEDLY PROVIDED A FALSE NEGATIVE READING WHEN USED ON THEIR 12-MONTH-OLD SON. THE DEVICE ALLEGEDLY DISPLAYED A TEMPERATURE OF 99.5°F, ALTHOUGH THE CHILD WAS LATER FOUND TO HAVE AN ACTUAL FEVER OF 105°F. THE CHILD SUBSEQUENTLY EXPERIENCED A FEBRILE SEIZURE, AND EMERGENCY SERVICES WERE CALLED. A PARAMEDIC CONFIRMED THE 105°F TEMPERATURE UPON ARRIVAL. THE CONSUMER STATED THAT THE THERMOMETER HAD BEEN USED ONCE PREVIOUSLY AND APPEARED TO FUNCTION PROPERLY AT THAT TIME. SHE ALSO MENTIONED THAT SHE WORKS IN THE NURSING FIELD. THE CHILD'S CURRENT CONDITION WAS NOT REPORTED. KAZ USA, INC. HAS REQUESTED THAT THE PRODUCT BE RETURNED TO OUR COMPANY FOR TESTING.
Patient problems: Convulsion/Seizure; Fever
MAUDE report 24918611 ↗MalfunctionAug 28, 2024False Negative Result; False Negative Result
A CONSUMER REPORTED THAT HER THERMOMETER HAD ALLEGEDLY GIVEN A FALSE NEGATIVE READING ON HER FIVE-MONTH-OLD SON. THE DEVICE ALLEGEDLY GAVE READINGS OF 96°F AND 98°F. THE CHILD WAS TAKEN TO A HOSPITAL WHERE A RECTAL TEMPERATURE OF 103.6°C AND THE PRESENCE OF CORONA VIRUS WAS CONFIRMED. THERE WERE NO COMPLICATIONS FROM THIS INCIDENT, AND THE PATIENT IS DOING WELL NOW. KAZ USA, INC. HAS REQUESTED THAT THE PRODUCT BE RETURNED TO OUR COMPANY FOR TESTING.
Patient problems: Fever; Viral Infection
MAUDE report 20086919 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.