FDAJune 30, 2017device

731 Series Ventilators running software version 05.20.00 The devices in the ZOLL ventilator are indicated for use in the management of infant through adult patients weighing ;:: 5 kg with acute or chronic respiratory failure or during resuscitation by providing continuous positive-pressure ventil...

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

The hazard

A software anomaly in the 731 software version 05/20/00, was identified, which can lead to a user inadvertently changing device settings.

What to do

FDA enforcement status: Terminated

Brands named

zoll medicalzoll

Recall history

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

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731 Series Ventilators running software version 05.20.00 The devices in the ZOLL ventilator are indicated for use in the management of infant through adult patients weighing ;:: 5 kg with acute or chronic respiratory failure or during resuscitation by providing continuous positive-pressure ventil... — Recall Details · AllClear