FDA Device Intelligence
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Thermometer, Clinical Color Change

FDA product code FQZ · Class 1 · General Hospital

61
Registered devices
6
Adverse events
2
Recalls
14
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-05-10BearCare, Inc.There have been reports of skin burns to children wearing the device.
2013-07-10Medical Indicators, Inc.TempaDot products may have been mislabeled.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.