FDAJuly 27, 2016device

CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care.

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

The hazard

A software error on released software versions 1.6.12, 1.6.12F and 1.6.16 may give wrong time data to measurements.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

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

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