Steris Corporation has recalled 10 units of the Barco MNA with the HexaVue IP Integration System (Model MNA-6x0-H) because the supplier used an incorrect configuration file during manufacturing. This sub-recall is part of a larger investigation into adapter components that may not function as intended due to this setup error. Consumers should identify the affected devices by their specific serial numbers and contact Steris Corporation to coordinate the necessary corrective actions.
The use of an incorrect configuration file in the adapter components can lead to system integration errors or unexpected device behavior during medical procedures. There have been no reported injuries associated with this specific manufacturing batch.
This is a sub-recall of event RES 96885 involving incorrect configuration files used by the supplier.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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