CW120N

WIDE corporation · Model CW120N · UDI-DI 08809241513124

510(k) clearances

Adverse events

Recalls

Facilities

Description

CW120N LCD Monitor System is intended to be used in displaying and viewing digital medical images for review and analysis by trained medical practitioners. It is specifically designed for digital mammography applications and digital breast tomosynthesis applications.

Recalls

Date	Firm	Reason
2021-01-22	Barco N.V.	A number of MDNC-3421 displays were shipped while not being DICOM-compliant. These displays will not pass DICOM acceptance tests.
2019-07-30	Eizo Corporation	Under certain conditions, a marble pattern infrequently appears on the monitor.
2019-07-30	Eizo Corporation	Under certain conditions, a marble pattern infrequently appears on the monitor.
2015-07-07	Eizo Corporation	EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort.
2015-07-07	Eizo Corporation	EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort.
2015-07-07	Eizo Corporation	EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.