FDA Slaps Covidien plc Ventilator With A Class I Recall Tag

The FDA issues a Class I recall for Covidien’s Puritan Bennett 840 ventilator due to a software problem. The FDA issued a Class I recall for Covidien’s (NYSE:COV) Puritan Bennett 840 Series Ventilator, because of a software issue that could cause the device to shut down. The Puritan Bennett ventilator is a critical care ventilator for adults, children and infants.

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