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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71628

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 07, 2015
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Eizo Corporation

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 690592034752. This product is intended to be used in displaying and viewing digital images including those of digital mammography for review and analysis by trained medical practitioners.

Z-2087-2015
Recall number
Z-2087-2015
Initiated
July 07, 2015
Classification
Class II
Status
Terminated
Recalling firm
Eizo Corporation
Quantity
19 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

21839093 21840093 21841093 21845093 21849093 21850093 21851093 21855093 21856093 21861093 23641024 24340064 24343064 24347064 24358064 24359064 24368064 24728094 24736094 25103104 25104104 25127104 25129104

Distribution pattern

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

device · product 2 of 3

RadiForce RX650, 6MP Color LCD Monitor, Part Code No. 0FTD1957A5, 0FTD195B5, UPC 690592037203. This product is intended to be used in displaying and viewing digital images for review and analysis by trained medical practitioners. It does not support the display of mammography images for diagnosis.

Z-2088-2015
Recall number
Z-2088-2015
Initiated
July 07, 2015
Classification
Class II
Status
Terminated
Recalling firm
Eizo Corporation
Quantity
3 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

20326034, 20618064, 20671064

Distribution pattern

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

device · product 3 of 3

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.

Z-2089-2015
Recall number
Z-2089-2015
Initiated
July 07, 2015
Classification
Class II
Status
Terminated
Recalling firm
Eizo Corporation
Quantity
2 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

220045044, 20050044

Distribution pattern

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