Oridion Medical recalls CAPNOSTREAM 20P patient monitors that may reset to factory default settings when powered off. Affected units have specific part numbers listed in the recall notice. No immediate action is required but users should check their device 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 certain CAPNOSTREAM 20P patient monitors that may reset to factory default settings when powered off. This could cause the monitor to lose custom settings like date/time, nurse call, and alarm configurations. The recall does not require immediate action but users should check their device settings to ensure they are not resetting.
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 lose custom configurations that healthcare providers set, such as specific alarm thresholds or call settings.
Healthcare providers using the CAPNOSTREAM 20P patient monitors with the specific part numbers listed in the recall notice are most at risk. Patients using these monitors may experience temporary loss of custom settings.
Check if your CAPNOSTREAM 20P patient monitor has a part number listed in the provided sequence (e.g., B632123514, B632123522, etc.). The recall covers specific units manufactured with these part numbers.
Verify that your monitor's date/time, nurse call, and alarm settings are not reset to factory defaults after being powered off.
No, the recall does not require stopping use. However, you should check your device settings to ensure they are not resetting to factory defaults.
The affected units have specific part numbers listed in the recall notice, including B632123514, B632123522, and other numbers provided in the sequence.
Check if your CAPNOSTREAM 20P monitor has a part number from the list of specific numbers provided in the recall notice.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0021-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0021-2019 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.
