United StatesNOxBOXi Nitric Oxide Delivery System (Model NOXBOX-I; manufacturer NOXBOXI/ NBL; U.S. distributor REQNOXBOXI/Linde; UDI‑DI 05060541640009; all serial numbers) sold in Tennessee is affected. The devices were recalled because an unexpected internal fault/system diagnostic error can result when a rapid succession of button selections is made on the user interface without waiting for the device to respond to prompts.
What's being recalled
NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
Recalling firm: Noxbox LTD, Sittingbourne, United Kingdom.
How to identify it
Model Numbers: (1) NOXBOXI (NBL (Manufacturer)), (2) REQNOXBOXI (Linde (U.S. Distributor)); UDI-DI: 05060541640009; All serial numbers.
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
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Domestic: TN;
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)