Precision Valve & Automation,Inc: Medical Device Recalls in 2020

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Precision Valve & Automation,Inc in 2020. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

2020

PVA, PREVENT is an FDA-authorized emergency ventilator designed to treat patients suffering from COVID-19 respiratory failure. This motorized device automatically compresses a resuscitator bag to provide air to the lungs of a COVID-19 patient, eliminating the human error and fatigue that results from manual actuation. PREVENT is indicated for emergency resuscitation with appropriate patient monitoring on adult patients that require mechanical respiratory support.