Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory defaults when powered off, potentially causing alarm settings to malfunction. Affected units include specific model numbers listed in the recall notice.
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 Capnostream20 bedside patient monitors that may reset to factory default settings when powered off. This could cause alarm settings to malfunction, potentially leading to missed critical patient alerts if the monitor is not properly configured.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could cause the monitor to not alert healthcare staff to critical patient conditions if the settings were adjusted for specific patient needs.
Healthcare professionals using Capnostream20 bedside monitors for patient monitoring are most at risk. Patients in hospitals or clinics using these monitors could be affected if settings reset unexpectedly.
Check for model numbers listed in the recall notice: B300001030, B300001023, and other specific serial numbers provided in the record. The product is sold internationally under the brand Oridion Medical.
Verify that the date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
The recall is happening because the Capnostream20 monitors may reset to factory default settings when powered off, which could cause alarm settings to malfunction.
Affected model numbers include B300001030, B300001023, and other specific serial numbers listed in the recall notice.
No, the recall does not require stopping use. Users should check settings after powering off the monitor to ensure they are not reset to factory defaults.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0044-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0044-2019 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.
