Z-2089-2015 Class II Terminated

Recalled by Eizo Corporation — Hakusanshi, N/A

FDA device recall Z-2089-2015 was initiated by Eizo Corporation on July 7, 2015 and is designated Class II. Reason for recall: EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort. The recall status is terminated (terminated November 30, 2016). Affected quantity: 2 units.

Recall Details

Product Type
Devices
Report Date
July 22, 2015
Initiation Date
July 7, 2015
Termination Date
November 30, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2 units

Product Description

RadiForce RX850, 8MP Color LCD Monitor, Part Code No. 0FTD1958A2, UPC 690592037180. This product is intended to be used in displaying and viewing digital images those of digital mammography for review and analysis by trained medical practitioners.

Reason for Recall

EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort.

Distribution Pattern

Nationwide Distribution including OH, FL, IL, TX, OH, NY, AZ, and NJ.

Code Information

220045044, 20050044