Noxbox Ltd medical device recall: NOxBOXi Nitric Oxide Delivery System
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Medical devices
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 97516
- Recall initiated
- Sep 9, 2025
- Classified by FDA
- Oct 6, 2025
- Posted in Enforcement Report
- Oct 15, 2025
- Recalling firm
- NOXBOX LTD
- Firm location
- Sittingbourne, United Kingdom
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Letter
- Products in this event
- 1
What to do
Compare the product, lot or serial numbers below with what you have. If you use a prescription drug or medical device in this recall, talk to your pharmacist or health care provider before you stop using it, and follow the firm's instructions.
Reason for recall
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 the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Sep 9, 2025. FDA classified it 27 days later, on Oct 6, 2025. Distribution reported by FDA: Domestic: TN; NOXBOX LTD has 6 recalls in our records.
Recalled products (1)
Z-0029-2026 Class I Ongoing
NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
Codes / lots: Model Numbers: (1) NOXBOXI (NBL (Manufacturer)), (2) REQNOXBOXI (Linde (U.S. Distributor)); UDI-DI: 05060541640009; All serial numbers.
Quantity: 1667 units
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA device enforcement dataset
- Official notice
- FDA Enforcement Report, event 97516
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.