FDA recall Z-0028-2026

NOXBOX LTD · Class I · device

Product

NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I

Reason for recall

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).

Distribution

Domestic: TN

Key facts

Status
Ongoing
Initiation date
2025-09-09
Report date
2025-10-15
Voluntary/Mandated
Voluntary: Firm initiated
Location
Sittingbourne, United Kingdom

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0028-2026