Eizo RadiForce GX540 Monitors Recalled for Display Abnormalities
Eizo is recalling 19 RadiForce GX540 monitors that may display abnormally when connected to specific graphics boards with DisplayPort.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically indicates a situation where use of the product may cause temporary or medically reversible health consequences, or where the probability of serious adverse health consequences is remote. No injuries or illnesses are reported in the source text.
Plain-English summary
Eizo Corporation is recalling 19 units of the RadiForce GX540, 5MP Monochrome LCD Monitor. The affected units are identified by Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, and UPC 690592034752. These monitors are intended for displaying and viewing digital images, including digital mammography, for review and analysis by trained medical practitioners.
The recall was initiated because the monitors could display abnormally while connecting to particular graphics boards with DisplayPort. The affected units were distributed nationwide, including in Ohio, Florida, Illinois, Texas, New York, Arizona, and New Jersey.
Consumers and medical facilities should stop using the affected monitors and contact Eizo Corporation for further instructions on the recall.
The recalled product
- Product
- 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…
- Manufacturer
- Eizo Corporation
- Hazard
- Affected units
- 19
Distribution
Part of a larger recall action
This product is one of 3 recalled by Eizo Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
Same manufacturer · Eizo Corporation
See all →- ModerateEizo RadiForce RX360 Medical Monitor Recalled for Display Defect
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