Orid: Capnostream20 bedside monitors may reset to factory defaults when powered off. Affected units include specific model numbers and refurbished versions.
The date/time, nurse call and alarm settings of the bedside patient monitors may reset to the factory default settings when the monitor is powered off.
Oridion Medical is recalling certain refurbished Capnostream20 patient monitors because their settings can reset to factory defaults when the device is powered off. This could lead to incorrect patient monitoring if the settings are not properly configured after power-off.
When the monitor is powered off, the date/time, nurse call, and alarm settings can reset to factory defaults. This could cause incorrect patient monitoring if the settings are not manually adjusted after power-on.
Healthcare workers using the Capnostream20 monitors for patient monitoring are most at risk if the device resets settings during power-off. Patients using these monitors may experience incorrect readings if settings are reset.
Check for model numbers B200001309, B200001965, B200001922, B200001084, or B200001075 on the device. The product is a refurbished Capnostream20 monitor.
Verify that the date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
The monitor settings may reset to factory defaults when powered off, which could lead to incorrect patient monitoring if settings are not manually adjusted.
The affected model numbers are B200001309, B200001965, B200001922, B200001084, and B200001075.
The recall does not require returning the monitor; users should check settings after power-off.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0051-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0051-2019 from Oridion 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.
