FDAJune 2, 2022device

Vivo 45LS Ventilator- intended to provide continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation Model Number: 230000 ¿ If the recalled product is a software, include version number: firmware versions 5.0.5 or earlier

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

The hazard

A forced shutdown of one of the processors did not generate a watch dog alarm, would develop into a failure AND the instructions to monitor a ventilator dependent patient are NOT followed, the health consequences could potentially be Permanent impairment or life threatening if medical intervention is not obtained

What to do

FDA enforcement status: Ongoing

Brands named

breas medicalbreas

UPCs

07321822300004

Recall history

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

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