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Braun

KAZ USA, INC. · Model PRO6000BSNAV2 · UDI-DI 00328785000511

FLL
10
510(k) clearances
1,303
Adverse events (13 deaths)
18
Recalls
479
Facilities

Description

Braun Thermoscan PRO6000 Accessory Thermometry, Charging Station, to be used with PRO6000 ear thermometer.

Recalls

DateFirmReason
2025-09-17Baxter Healthcare CorporationAffected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower temperature than the true value, w
2024-06-13Baxter Healthcare CorporationThe Braun Thermoscan PRO 6000 ear thermometers may have been shipped with a compact disc (CD) containing an outdated version of the Instructions for Use (IFU).
2021-07-20Welch Allyn IncIf the device is exposed to fluid ingress and is used before the cleaning fluid has completely dried, there is a risk of the device overheating potentially causing a burn to the us
2019-10-28Cardinal Health 200, LLCThe frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (
2019-10-28Cardinal Health 200, LLCThe frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (
2019-10-28Cardinal Health 200, LLCThe frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (
2019-10-28Cardinal Health 200, LLCThe frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (
2019-10-28Cardinal Health 200, LLCThe frequency of calibration for the Genius Tympanic Thermometer as stated in the operating manual may not ensure that thermometers always remain within the stated accuracy range (
2018-02-02Philips Consumer LifestyleDevice may provide inaccurate measurements.
2017-10-173M Company - Health Care BusinessDuring a recent investigation, 3M confirmed that a programming translation error could occur in a small amount of the sensors that could lead to a temperature readout that is lower

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.