FDASeptember 9, 2025device
NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The unexpected internal fault / system diagnostic error to result when a rapid succession of button selections is made to the user interface without waiting for the device to respond to user prompts.
What to do
FDA enforcement status: Ongoing
Brands named
noxbox
UPCs
05060541640009
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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