FDAJanuary 23, 2015device

Passport V Monitor, Multiparameter Patient Monitor(with Arrhythmia Detection and Alarms) Intended for intra hospital use under the direct supervision of a licensed healthcare practitioner.

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

The hazard

An issue has been identified with Passport V Monitors invasive blood pressure function (IBP) which may provide an incorrect IBP measurement

What to do

FDA enforcement status: Terminated

Brands named

mindray ds usa inc dba mindray north americamindraymindray ds

Recall history

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

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