Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2294-2020 — RadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The display is not intended for mammography.

U.S. FDA — Device Enforcement · Japan · 2019-07-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2294-2020
Date of alert
2019-07-30
Country / jurisdiction
Japan
Risk level
Class II
Risk type
recall
Brand
Eizo Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04995047053279
Reported risk: Under certain conditions, a marble pattern infrequently appears on the monitor.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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