Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory settings when powered off, potentially affecting patient safety 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 CAPNOSTREAM 20P bedside patient monitors because their settings may reset to factory defaults when the monitor is powered off. This could lead to incorrect patient monitoring if the device is not properly configured after power cycles.
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 if the device is not properly configured after power cycles, potentially leading to missed alarms or incorrect patient data.
Healthcare professionals using the CAPNOSTREAM 20P monitors in hospitals or clinics are most at risk, as improper settings could affect patient monitoring.
The recalled product is the CAPNOSTREAM 20P (INTL) N W/PRINTER model with the serial numbers listed in the recall notice. These monitors were sold internationally with the specific model identifiers mentioned.
Verify that the date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
The monitor settings may reset to factory defaults when powered off, which could lead to incorrect patient monitoring if not properly configured.
No, but you should check the settings after powering off the monitor to ensure they are not reset to factory defaults.
Check the monitor settings after powering off to ensure they are not reset to factory defaults. If settings are reset, you may need to reconfigure them.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0056-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0056-2019 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.
