Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

HAMILTON-H900 Humidifier Recalled by Hamilton Medical AG Due to When starting a humidifier, intended for respiratory gas...

Date: January 5, 2021
Company: Hamilton Medical AG
Status: Completed
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Hamilton Medical AG directly.

Affected Products

HAMILTON-H900 Humidifier, Models: 950001, 950004

Quantity: 203

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 6 states: CA, FL, NV, PA, TX, WI

Affected (6 states)Not affected

About Hamilton Medical AG

Hamilton Medical AG has 12 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report