CLASS II Device recall · Reported 22 Jul 2015 · FDA Enforcement Report

RadiForce GX540, 5MP Monochrome LCD Monitor, Part recalled by Eizo

Eizo is recalling RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, distributed nationwide in the US. The recall was initiated on 7 Jul 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes21839093 21840093 21841093 21845093 21849093 21850093 21851093 21855093 21856093 21861093 23641024 24340064 24343064 24347064 24358064 24359064 24368064 24728094 24736094 25103104 25104104 25127104 25129104

Quantity recalled19 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2087-2015
FDA event ID: 71628
Recalling firm: Eizo, Hakusanshi, N/A
Classification: Class II
Status: Terminated
Recall initiated: 7 Jul 2015
FDA classified: 16 Jul 2015
Reported: 22 Jul 2015
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Imaging Equipment

Timeline

7 Jul 2015	Recall initiated by company
16 Jul 2015	Classified by FDA	+9 days
22 Jul 2015	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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.

Where it was distributed

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

Nationwide Arizona Florida Illinois New Jersey New York Ohio Texas

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it sold?

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

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 71628

Reported	Class	Recall	Company	Reason	Where
22 Jul 2015	CLASS II	RadiForce RX650, 6MP Color LCD Monitor, Part recalled by Eizo	Eizo	Device Malfunction	Nationwide
22 Jul 2015	CLASS II	RadiForce RX850, 8MP Color LCD Monitor, Part recalled by Eizo	Eizo	Other	Nationwide

More recalls from Eizo

All 5

Reported	Class	Recall	Company	Reason	Where
17 Jun 2020Device	CLASS II	RadiForce RX360 recalled by Eizo	Eizo	Other	Nationwide
17 Jun 2020Device	CLASS II	RadiForce GX560 monochrome LCD monitor recalled by Eizo	Eizo	Other	Nationwide
22 Jul 2015Device	CLASS II	RadiForce RX850, 8MP Color LCD Monitor, Part recalled by Eizo	Eizo	Other	Nationwide
22 Jul 2015Device	CLASS II	RadiForce RX650, 6MP Color LCD Monitor, Part recalled by Eizo	Eizo	Device Malfunction	Nationwide

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