Oridion Medical recalls CAPNOSTREAM 20 (US) N patient monitors with part numbers CS08651 and others due to potential reset of date/time, nurse call, and alarm settings when powered off. Affected units may need verification.
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 CAPNOSTREAM 20 (US) N patient monitors because their date/time, nurse call, and alarm settings can reset to factory defaults when the monitor is powered off. This could cause incorrect patient monitoring settings to be used during medical care.
When the monitor is powered off, the date/time, nurse call, and alarm settings can reset to factory defaults. This means the monitor might not function correctly when turned back on, potentially leading to incorrect patient monitoring settings.
Healthcare providers using the CAPNOSTREAM 20 (US) N patient monitors with specific part numbers listed in the recall. Patients using these monitors are at low risk as the issue doesn't cause immediate harm.
Check if your CAPNOSTREAM 20 (US) N patient monitor has part numbers listed in the recall (e.g., CS08651, B200001468, B200001473, etc.).
Look for the part number on your CAPNOSTREAM 20 (US) N patient monitor to see if it matches the list of affected part numbers provided in the recall.
The recall includes CAPNOSTREAM 20 (US) N patient monitors with part numbers listed in the record, such as CS08651, B200001468, B200001473, and others.
If your monitor's part number is not listed in the recall, it is not affected and no action is needed.
The issue could cause the monitor to reset settings when powered off, potentially leading to incorrect patient monitoring settings when the monitor is turned back on.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0020-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0020-2019 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.
