O-Two Medical recalls Equinox Relieve N2O/O2 mixing system model 01EQ1000 due to potential higher nitrous oxide delivery than specified. Affected units have serial numbers EQ1332-17 to EQ3003-18.
Higher levels of nitrous oxide delivered than specification
O-Two Medical recalls its Equinox Relieve N2O/O2 analgesic gas system model 01EQ1000 because it may deliver higher levels of nitrous oxide than intended. This could lead to unintended medical effects if used improperly.
The system may deliver more nitrous oxide than specified, which could cause unintended medical effects like over-sedation or respiratory issues if used without proper monitoring.
Patients using the O-Two Equinox Relieve system for medical nitrous oxide delivery are affected. Those with medical conditions requiring precise gas concentrations are at higher risk.
Check for model number 01EQ1000 on the device. Affected units have serial numbers EQ1332-17 through EQ3003-18.
Look for model number 01EQ1000 on the device to confirm it is affected.
The recall indicates a potential risk of higher nitrous oxide delivery than specified, so it is not recommended for use until the remedy is applied.
Check the model number and serial number to see if it is affected; if so, stop using it and contact O-Two for guidance.
The recall record does not specify a remedy, so O-Two may need to be contacted directly for assistance.
We’ve drafted a message you can send O-Two to request your refund or repair — edit it as you like.
Subject: Recall Z-2885-2018 — O-Two O-Two Hello, I own a O-Two that is covered by recall Z-2885-2018 from O-Two. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
