Oridion Medical recalls Capnostream20 bedside monitors with part numbers CS08751 and others that may reset date/time and alarm settings to factory defaults when powered off. This could affect patient monitoring accuracy.
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 Capnostream20 bedside patient monitors that may reset date/time and alarm settings to factory defaults when powered off. This could lead to incorrect patient monitoring readings 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 incorrect patient monitoring readings if the monitor is not properly configured after power-off.
Healthcare professionals using the Capnostream20 monitors for patient monitoring are most at risk. The recall affects specific models sold in the U.S. with part numbers listed in the record.
Check for part numbers listed in the record, such as CS08751, B500002176, and other serial numbers provided in the recall notice. The monitors are sold in the U.S. for patient monitoring use.
Verify that date/time, nurse call, and alarm settings have not reset to factory defaults after powering off the monitor.
The monitor may reset date/time, nurse call, and alarm settings to factory defaults when powered off, which could lead to incorrect patient monitoring readings.
Check for part numbers listed in the recall, such as CS08751, B500002176, and other serial numbers provided in the record.
No action is needed if your monitor is not listed in the recall part numbers.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0031-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0031-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
