FDAJuly 13, 2017device

CARESCAPE Patient Data Module (PDM) v2.6 software used with CARESCAPE Monitors B850, B650, and B450 v2.0.7 or earlier software The PDM is intended to provide uninterrupted acquisition of physiologic parameter data on adult, pediatric and neonatal patients during non-transport/bedside and transpor...

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

The hazard

Device does not produce a visual or audible impedance respiration APN alarm when an impedance respiration apnea event occurs.

What to do

FDA enforcement status: Terminated

Brands named

ge medical systems information technologies

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →