Class II
Medical Device Recall: NOxBOXi Nitric Oxide Delivery System
NOXBOX LTD · July 19, 2023
Reason for Recall
Replacement of the internal Sample Pump due to high failure rates.
Distribution
US Nationwide distribution in the state of TN.
States Affected
NATIONWIDE
Quantity Affected
1,667 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2544-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.