Oridion Medical recalls CAPNOSTREAM 20 bedside monitors that may reset to factory defaults when powered off. Affected units have specific part numbers. No remedy is stated in the recall notice.
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 20 bedside patient monitors because their date/time, nurse call, and alarm settings can reset to factory defaults when the monitor is powered off. This could cause incorrect patient monitoring settings to be used, potentially leading to missed alarms or incorrect patient data.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory default values. This could result in incorrect patient monitoring settings being used, potentially causing missed alarms or inaccurate patient data.
Healthcare professionals using the CAPNOSTREAM 20 bedside monitors for patient monitoring are most likely affected. Patients using these monitors could be at risk if settings reset incorrectly.
Check for part numbers listed in the recall notice: B200001301 through B450124001. The product is the CAPNOSTREAM 20 (INTL) N model.
Verify that the date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
The affected part numbers are listed in the recall notice: B200001301 through B450124001.
The recall notice does not state any remedy for this issue.
Check if your monitor has a part number listed in the recall notice (B200001301 through B450124001).
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0036-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0036-2019 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.
