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Vicks VDT972BBUSRecalls & reported problems

Kaz USA, Inc. · TWO SECOND DIGITAL THERMOMETER W/ FEVER INSIGHT, FLEXIBLE TIP, F/C READINGS, PEDIATRIC PACKAGING · Class 2

All models of Vicks (12)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00328785001518), received between Sep 11, 2020 and Sep 11, 2020 — classified as 1 malfunction.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • False Negative Result1
  • Insufficient Device Problem Information1

Patient problems

  • Fever1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 11, 2020False Negative Result; Insufficient Device Problem Information; False Negative Result; Insufficient Device Problem Information

    A CONSUMER REPORTED THAT HIS THERMOMETER HAD ALLEGEDLY GIVEN FALSE NEGATIVE READINGS ON HER MOTHER. THE DEVICE ALLEGEDLY GAVE READINGS AROUND 92°F, AND A READING OF 102.5°F WAS LATER MEASURED AT A HOSPITAL. 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

    MAUDE report 10524995 ↗

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Sources and updates

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