Oridion Medical recalls certain Capnostream20 bedside monitors that may reset to factory defaults when powered off. This could affect patient monitoring 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 specific models of Capnostream20 bedside patient monitors that may reset to factory default 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 affecting patient safety.
Healthcare professionals using the recalled Capnostream20 monitors for patient monitoring are most at risk. Patients using these monitors could be affected if settings reset incorrectly.
Check for the part number CS78651 or the serial numbers listed in the recall notice. These monitors were refurbished and sold in the US.
Verify that the date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
The recall is happening because the date/time, nurse call, and alarm settings may reset to factory defaults when the monitor is powered off, which could lead to incorrect patient monitoring settings.
Check for the part number CS78651 or the serial numbers listed in the recall notice. These monitors were refurbished and sold in the US.
Verify that the date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0032-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0032-2019 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.
