Oridion Medical recalls CAPNOSTREAM 20P patient monitors that may reset to factory defaults when powered off. This could affect alarm and nurse call settings.
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 CAPNOSTREAM 20P patient monitors that may reset to factory default settings when powered off. This could cause alarm and nurse call settings to return to default values, potentially missing critical patient alerts.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could cause critical patient alerts to be missed if the settings are not properly configured after power-off.
Patients using the CAPNOSTREAM 20P patient monitors with the specified part numbers. Healthcare providers who use these monitors for bedside patient monitoring are most at risk.
Check the part numbers listed in the recall notice. The CAPNOSTREAM 20P (INTL) N - ROHS model with part numbers starting with B836141168 through P806176448.
Verify that date/time, nurse call, and alarm settings are correctly configured after powering off the monitor.
The CAPNOSTREAM 20P (INTL) N - ROHS model with part numbers from B836141168 to P806176448.
You can check if your monitor settings reset after power-off. If so, you may need to reconfigure the settings.
The recall indicates a potential for settings to reset, but no specific injuries have been reported. The risk is low.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0038-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0038-2019 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.
