Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that reset to factory settings when powered off. This may 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 its CAPNOSTREAM 20P bedside patient monitors because they may reset to factory settings when powered off. This could lead to incorrect patient monitoring settings being used, potentially affecting patient safety.
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 settings to be used, potentially leading to missed critical alerts or incorrect patient care.
Healthcare facilities using the CAPNOSTREAM 20P monitors are most at risk. Patients in hospitals or clinics with this monitor may experience inaccurate monitoring settings.
Check for the CAPNOSTREAM 20P (INTL) N W/PRINTER model with serial numbers listed in the recall notice. The product includes specific serial numbers starting with B819140013 through P806176472.
Verify that the date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
The monitor may reset to factory settings when powered off, which could cause incorrect patient monitoring settings to be used.
Check if your monitor has a serial number listed in the recall notice, which includes a range from B819140013 to P806176472.
Check the monitor settings after powering off to ensure they are not reset to factory defaults. If settings are reset, contact Oridion Medical for further instructions.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0042-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0042-2019 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.
