FDA recall Z-1966-2023

Vyaire Medical · Class II · device

Product

bellavista 1000 Ventilator, Catalogue Number 301.100.030; Continuous Use Ventilator

Reason for recall

Vyaire Medical identified two patient safety risks during the use of the bellavista 1000 and bellavista 1000e: 1. Under certain conditions of use, the touchscreen may become unresponsive and the device application stops responding (APP Hang). When this occurs, if the user continues to interact with the touchscreen, a message will appear that states DeviceSoftware.Application is not responding or a decommission screen will appear on the user interface. The ventilator will issue both an audible and visual alarm. Ventilation continues without interruption with the settings applied prior to the APP Hang error. 2. The potential for a use error has been identified if the operator applies the proposed settings without confirming the settings are suitable for the patient.

Distribution

US Nationwide Distribution

Key facts

Status
Completed
Initiation date
2023-05-05
Report date
2023-06-21
Voluntary/Mandated
Voluntary: Firm initiated
Location
Mettawa, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1966-2023