Recall company profile

NOXBOX LTD Recalls

Overview of recall records associated with NOXBOX LTD, including dates, categories and classifications where available.

3recall records
Oct 15, 2025latest record date
Jun 21, 2023earliest record date

Recall history in this database

Classification mix: Class I: 3.

Medical DeviceOct 15, 2025

NOXBOX recall — FDA Z-0028-2026

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…

Class IFDA: OngoingNOXBOX LTD
Medical DeviceOct 15, 2025

NOXBOX recall — FDA Z-0029-2026

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…

Class IFDA: OngoingNOXBOX LTD
Medical DeviceJun 21, 2023

NOXBOX recall — FDA Z-1667-2023

Device may experience malfunctions due to misalignment of the check valve in the manifold. If the device fails, there is a risk of nitric oxide leak, oxygen gas leak, or earlier cylinder…

Class IFDA: TerminatedNOXBOX LTD

Understanding this recall history

This page summarizes recall records in which the official source identifies NOXBOX LTD as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.