FDAAugust 31, 2018device

Solar 8000i Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.

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

The hazard

The patient monitors may simultaneously restart as designed if all are connected to the same network and a network overload occurs for a prolonged time.

What to do

FDA enforcement status: Ongoing

Brands named

ge healthcare

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 →