FDADecember 20, 2021device

bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. The bellavista 1000/1000e ventilator is intended to provide positive pressure ventilatory support to adult and pediatric patients, and optionally, infant and neonatal patients.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Potential cessation in ventilation can occur under specific conditions.

What to do

FDA enforcement status: Terminated

Brands named

vyaire medicalvyaire

UPCs

0764014938111507640149388879

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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