Oridion Medical recalls Capnostream20 bedside monitors that may reset to factory defaults 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 certain Capnostream20 bedside monitors that may reset to factory default settings when powered off. This could cause critical patient monitoring settings to revert, potentially leading to safety risks during medical use.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could cause critical patient monitoring settings to revert to unsafe defaults, potentially missing vital patient conditions.
Healthcare providers using the recalled Capnostream20 monitors are most at risk, as these devices are critical for patient monitoring in medical settings.
The recalled units are labeled as 'Capnostream20 (US) N W/PRINTER REFURBISHED' with part number CS78657. They were sold with serial numbers starting with B200001412 through B200001998 and B400002305 through B410123252.
Verify that the date/time, nurse call, and alarm settings do not reset to factory defaults when the monitor is powered off.
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 affect patient safety.
Your monitor is affected if it is labeled 'Capnostream20 (US) N W/PRINTER REFURBISHED' with part number CS78657 and has a serial number starting with B200001412 through B200001998 or B400002305 through B410123252.
The recall does not require immediate action, but you should check if the settings reset when powered off. If they do, contact Oridion Medical for further guidance.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0034-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0034-2019 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.
