Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory settings when powered off. This could affect patient monitoring accuracy. Contact Oridion for details.
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 Capn:stream20 bedside patient monitors that may reset to factory settings when powered off. This could lead to inaccurate patient monitoring readings if the monitor is not properly configured after power-off.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could cause inaccurate patient monitoring if the settings are not manually adjusted after power-on.
Healthcare professionals using Capnostream20 monitors for patient monitoring. Patients using these monitors are at low risk if the monitor is properly configured after power-off.
Check for the model number CS08796 on the monitor. The product was sold with serial numbers B500002484, B500002616, and B500002723.
After powering on, verify that the date/time, nurse call, and alarm settings are not reset to factory defaults.
The monitor may reset to factory settings when powered off, which could affect patient monitoring accuracy.
Check for the model number CS08796 on the monitor. The product was sold with serial numbers B500002484, B500002616, and B500002723.
After powering on, verify that the date/time, nurse call, and alarm settings 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-0048-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0048-2019 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.
