FDA recall record

Vyaire Medical bellavista 1000e Ventilator, Catalogue Number 301.100.130 recall — FDA Z-1967-2023

Vyaire Medical identified two patient safety risks during the use of the bellavista 1000 and bellavista 1000e: 1. Under certain conditions of use, the…

Class IIclassification
Z-1967-2023official record ID
Jun 21, 2023report date

Recall record at a glance

Official recordZ-1967-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusCompleted
Recalling firmVyaire Medical
Report dateJun 21, 2023
Recall initiation dateMay 5, 2023
Quantity392 units
LocationMettawa, IL, United States

Official product description

bellavista 1000e Ventilator, Catalogue Number 301.100.130; Continuous Use Ventilator

Why the product was recalled

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 information

US Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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