FDANovember 7, 2014device

Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care

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

The hazard

Unintended treatment termination could result from a keypad malfunction in some situations. The device erroneously interprets this as a Stop Treatment Instruction. An alarm will not sound, or be registered. Accessories and monitoring equipment connected to the Vivo 50 will stop functioning as the device enters stand-by mode.

What to do

FDA enforcement status: Terminated

Brands named

breas medical abbreasbreas medical

Recall history

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

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