Oridion Medical recalls CAPNOSTREAM 20 bedside monitors with part number CS08657 that reset date/time and alarm settings when powered off. Affected units may have incorrect settings after power cycles.
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 20 bedside patient monitors with part number CS08657. When these monitors are powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could lead to incorrect settings being used during patient monitoring.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory default settings. This could cause incorrect patient monitoring settings to be used after the monitor is powered on again, potentially leading to miscommunication or delayed responses to patient needs.
Healthcare facilities using Oridion CAPNOSTREAM 20 bedside monitors with part number CS08657 are most at risk. Patients using these monitors could experience incorrect settings if the device resets after power cycles.
Check if your CAPNOSTREAM 20 monitor has part number CS08657. This model includes specific serial numbers listed in the recall notice. The product was sold with certain serial numbers as detailed in the recall list.
Verify that the date/time, nurse call, and alarm settings are correct after powering on the monitor. If they reset to factory defaults, contact Oridion Medical.
The part number for the recalled CAPNOSTREAM 20 monitors is CS08657.
No, the recall does not require immediate discontinuation. However, you should check the settings after powering on the monitor to ensure they are correct.
Check if your monitor has part number CS08657. Affected units have specific serial numbers listed in the recall notice.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0024-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0024-2019 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.
