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Hamilton Medical AG recalls HAMILTON-H900 Humidifier, Models: 950001, 950004
Recalled July 20, 2022 · FDA recall Z-1385-2022 · Hamilton Medical AG
Hazard
When starting a humidifier, intended for respiratory gas conditioning during invasive and noninvasive mechanical ventilation, with an empty chamber, and water is not filled into the chamber, the low water level alarm will be delayed and medical staff are unaware that there is no water in the chamber. · FDA Class III
Units
203
Sold at
US: WI, FL, CA, NV, PA, TX, PA
Description
When starting a humidifier, intended for respiratory gas conditioning during invasive and noninvasive mechanical ventilation, with an empty chamber, and water is not filled into the chamber, the low water level alarm will be delayed and medical staff are unaware that there is no water in the chamber.
Product
HAMILTON-H900 Humidifier, Models: 950001, 950004
Manufacturer(s)
Hamilton Medical AG
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →