GE Healthcare Finland Oy recalls GE Healthcare CARESCAPE Monitor B650

Recall date

May 25, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2340-2018

FDA classification

Class II

Brand / firm

GE Healthcare Finland Oy

Sold / distributed

worldwide

Why it was recalled

When multiple CARESCAPE Monitor B650 units are connected to the same network and a network overload occurs for a prolonged time, the monitors may simultaneously restart as designed. The monitor restart will not be completed until the network issue has been corrected.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

GE Healthcare CARESCAPE Monitor B650