FDA Device recall Z-1667-2023
NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device
- FDA Device
- Class I
- terminated
- Published 2023-06-21
On 2023-06-21 the FDA classified a Class I recall of NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device by Noxbox, citing 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 c….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1667-2023 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2023-05-03 |
| Published | 2023-06-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Noxbox |
| Distribution | US |
Product
NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device
Reason
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 changeover than expected or not at all. In a worst case scenario, there may be an interruption in therapy which could lead to oxygen desaturation of the patient and associated complications.
Identifiers
| code_info | UDI/DI: 5060541640009 Serial Numbers distributed in US: NI101029 NI102476 NI102518 NI102560 NI102594 NI102629 NI10138…UDI/DI: 5060541640009 Serial Numbers distributed in US: NI101029 NI102476 NI102518 NI102560 NI102594 NI102629 NI101388 NI102477 NI102519 NI102561 NI102595 NI102630 NI101392 NI102478 NI102520 NI102562 NI102596 NI102631 NI101441 NI102479 NI102522 NI102563 NI102597 NI102632 NI101562 NI102480 NI102525 NI102564 NI102598 NI102633 NI101679 NI102481 NI102528 NI102565 NI102599 NI102634 NI101703 NI102482 NI102530 NI102567 NI102600 NI102635 NI101760 NI102483 NI102531 NI102569 NI102601 NI102636 NI101806 NI102484 NI102535 NI102571 NI102602 NI102637 NI101881 NI102485 NI102537 NI102573 NI102604 NI102639 NI101927 NI102486 NI102538 NI102574 NI102605 NI102640 NI102024 NI102487 NI102539 NI102575 NI102606 NI102641 NI102097 NI102493 NI102540 NI102576 NI102608 NI102642 NI102111 NI102495 NI102541 NI102577 NI102610 NI102646 NI102193 NI102496 NI102542 NI102578 NI102611 NI102647 NI102255 NI102497 NI102544 NI102579 NI102613 NI102649 NI102311 NI102498 NI102545 NI102580 NI102614 NI102652 NI102394 NI102499 NI1025 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1667-2023%22
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