RegWardenFDA facility compliance records
Facility

EIZO GmbH

2 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2015: 1 recalls; 2018: 1 inspections; 2019: 1 recalls; 2023: 1 inspections1201520162017120181201920202021202212023202420252026
  • Recalls (2)
  • Inspections (2)

Devices registered here (1)

  • Display, Cathode-Ray Tube, Medical
    Product code DXJ (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.2450

Recalls & enforcement

  • Class IIOngoing2019-07-30
    Under certain conditions, a marble pattern infrequently appears on the monitor.
  • Class IITerminated2015-07-07
    EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort.

FDA inspections (2)

  • NAI2023-01-20
    No Action Indicated · Compliance: Devices
  • NAI2018-09-20
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “EIZO GmbH (FEI 3006615345) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006615345-eizo-gmbh/

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