Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0028-2026 — NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I

U.S. FDA — Device Enforcement · United Kingdom · 2025-09-09 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0028-2026
Date of alert
2025-09-09
Country / jurisdiction
United Kingdom
Risk level
Class I
Risk type
recall
Brand
NOXBOX LTD
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
05060541640009
Reported risk: Fluctuations may be more likely to occur if the total flow through the device sensor (used by the device to determine flow) is less than the minimum device requirement of 0.5 LPM. In addition, dose fluctuations have been observed when Bunnel LifePulse HFJV system or conventional ventilators have the following device settings: low service pressures generally less than 3.0 PSI, a pressure difference greater than 5.0cm H2O; or at breath per minute rates of 300 (5 Hz).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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