FDA Device recall Z-2885-2018
O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000
- FDA Device
- Class II
- terminated
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000 by O Two Medical Technologies, citing higher levels of nitrous oxide delivered than specification.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2885-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-14 |
| Published | 2018-08-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | O Two Medical Technologies |
| Distribution | AK, CA, FL |
Product
O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000
Reason
Higher levels of nitrous oxide delivered than specification
Identifiers
| code_info | Serial Number: EQ1332-17, EQ3001-18, EQ3003-18 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2885-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.