Drug recall
NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device
FDA recall event 92171 · Class I · NOXBOX LTD
Key facts
| Event ID | 92171 |
|---|---|
| Recall numbers | Z-1667-2023 |
| Recalling firm | NOXBOX LTD |
| Product type | Devices |
| Products | NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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 gas… |
| Initiation date | May 3, 2023 |
| Report date | Jun 21, 2023 |
| Termination date | Oct 31, 2024 |
| City | Sittingbourne |
| Country | United Kingdom |
| FEI number | 3012796317 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: