Noxbox Ltd: Noxboxi Nitric Oxide Delivery System. Model Number: Noxbox-i
NOxBOXi Nitric Oxide Delivery System Recall Summary NOXBOX LTD is recalling the NOxBOXi Nitric Oxide Delivery System (Model NOXBOX-I) due to a manufacturing defect in certain oxygen sensors that can cause inaccurate oxygen readings. The device has been distributed nationwide across all states. This is a Class II recall, indicating a potential serious health hazard from the inaccurate readings.
- Recalling firm
- NOXBOX LTD
- Product
- NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I.
- Reason
- Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-09-14
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the state of Georgia.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/27e1fce6-29a4-4659-b80b-865792684ced