Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory defaults when powered off. Affected units have specific serial numbers. No immediate action needed but check settings after power cycles.
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 bedside patient monitors that may reset to factory default settings when powered off. This could cause incorrect alarm or nurse call settings to be restored, potentially leading to missed patient alerts if the monitor is not functioning properly.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could result in incorrect alarm thresholds or missed patient alerts if the monitor is not properly configured after power cycles.
Patients using the CAPNOSTREAM 20P bedside monitors with the specific serial numbers listed in the recall. Healthcare providers who manage these monitors are most at risk of potential misconfiguration.
Check for the CAPNOSTREAM 20P (INTL) N W/PRINTER model with the specific serial numbers listed in the recall notice. The product includes the ROHS compliance identifier CS08658-03.
After powering the monitor on, verify that the date/time, nurse call, and alarm settings are correct and not reset to factory defaults.
No, the recall does not require immediate discontinuation. Check settings after power cycles to ensure they are correct.
The recall lists specific serial numbers starting with PA14170895 through PA24172455, but the full list is provided in the official notice.
The recall does not mention a fix or remedy. Users should check settings after power cycles to ensure they are correct.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0043-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0043-2019 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.
