FDA Recall Completed

HAMILTON-H900 Humidifier, Models: 950001, 950004

Recall: Z-1385-2022 · Initiated January 5, 2021

Recall

Recall Number
Z-1385-2022
Event Number
90460
Firm
Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland
FEI Number
3001421318
Product Code
BTT
Status
Completed
Root Cause
Employee error
Initiated
January 5, 2021

Description

HAMILTON-H900 Humidifier, Models: 950001, 950004

Reason

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.

Action

On 01/05/21, Field Safety Corrective Action notices were sent to customers who were asked to do the following: Follow the instructions in the HAMILTON-H900 Operator s Manual 624431 section 3.4. Before connecting a new patient to the humidifier; " Verify that the alarms operate correctly. " Ensure that the water supply to the humidifier chamber is functioning properly. Distribute this notification to all end users within your organization. A Medical Representative will be in contact to schedule service with a software update. Customers with additional questions or concerns were encouraged to call Technical Support at 1-800-426-6331, option #2.

Distribution

US: WI, FL, CA, NV, PA, TX, PA

Quantity

203