NOX Medical recalls T3s recorders with firmware error causing inaccurate device position detection during sleep monitoring. Affected units have specific serial numbers. No action required as the issue does not pose a safety risk.
Error in the device firmware results in the inaccurate detection of device position.
NOX Medical is recalling T3s recorders that may inaccurately detect device position during sleep monitoring. This could lead to incorrect health data readings but does not pose a safety risk to users.
The device firmware error causes the T3s recorder to misread its position during sleep. This may result in incorrect physiological signal data being recorded, but does not cause physical harm or safety issues.
People who own or use the NOX T3s Recorder for sleep monitoring are affected. Those with the specific serial numbers listed in the recall are most at risk of inaccurate health data readings.
Check if your NOX T3s Recorder has a serial number starting with 300106 (e.g., 300106423, 300106426). The device is intended for sleep monitoring and may have a specific catalog number.
Verify your NOX T3s Recorder's serial number matches the list provided in the recall notice.
No, the recall states the issue does not pose a safety risk. The firmware error may cause inaccurate health data but does not cause physical harm.
No action is required. The recall does not include a remedy, and the device is safe to use as the issue does not affect safety.
The affected units have serial numbers starting with 300106, such as 300106423, 300106426, and others listed in the recall notice.
We’ve drafted a message you can send NOX MEDICAL to request your refund or repair — edit it as you like.
Subject: Recall Z-0031-2022 — NOX MEDICAL NOX MEDICAL Hello, I own a NOX MEDICAL that is covered by recall Z-0031-2022 from NOX MEDICAL. 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.
