Oridion Medical recalls refurbished Capnostream20 bedside monitors that may reset to factory settings when powered off. This could affect patient monitoring accuracy. Affected units have specific part 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 refurbished Capnostream20 bedside monitors that may reset to factory settings when powered off. This could cause patient monitoring settings to be incorrect, 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 lead to incorrect patient monitoring settings, potentially affecting patient safety.
Healthcare professionals using the Capnostream20 bedside monitors in hospitals or clinics. Patients using these monitors are at risk if settings reset incorrectly.
Check for part numbers listed in the recall: B300001025 through B500002231. The monitors are refurbished models with the specific part numbers provided.
Verify that 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 affect patient monitoring accuracy.
Affected part numbers include B300001025 through B500002231 as listed in the recall notice.
The recall does not require returning the monitor; users should check settings 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-0033-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0033-2019 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.
