Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory settings when powered off. This could affect patient monitoring accuracy. Affected units have specific serial numbers.
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 Capnostream20 bedside monitors that may reset to factory settings when powered off. This could lead to inaccurate patient monitoring settings, 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 when the monitor is powered on again.
Healthcare professionals using the Capnostream20 bedside monitors for patient monitoring are most at risk. Patients using these monitors could be affected if settings reset.
Check for the model name 'Capnostream20 (INTL) M W/PRINTER REFURBISHED' and serial numbers listed in the recall notice: B300001456, B300001184, B500002163, B500002232, B300001007, B300001120, B300001148, B300001251.
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 inaccurate patient monitoring.
Check for the model name 'Capnostream20 (INTL) M W/PRINTER REFURBISHED' and the specific serial numbers listed in the recall notice.
The recall does not specify a remedy, so check the monitor settings after powering off to ensure they are not reset to factory defaults.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0054-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0054-2019 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.
