Eizo RadiForce RX650 LCD Monitor Recalled for Display Abnormalities
Eizo is recalling RadiForce RX650 LCD monitors that may display abnormally when connected to specific graphics boards using 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 the RadiForce RX650 6MP Color LCD Monitor. The recall involves 3 units of the product, which is intended for displaying and viewing digital images for review and analysis by trained medical practitioners. The product does not support the display of mammography images for diagnosis.
The recall is being conducted 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 practitioners should stop using the affected monitors and contact Eizo Corporation for further instructions or a remedy.
The recalled product
- Product
- 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…
- Manufacturer
- Eizo Corporation
- Hazard
- Affected units
- 3
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- 20326034
- 20618064
- 20671064
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
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