Oridion Medical recalls CAPNOSTREAM 20P bedside patient monitors that may reset date/time, nurse call, and alarm settings to factory defaults when powered off. This could affect patient monitoring safety.
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 20P bedside patient monitors that may reset date/time, nurse call, and alarm settings to factory defaults 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 result in incorrect patient monitoring settings being used, which might affect patient safety.
Patients using bedside monitors with this model may be affected if the monitor resets settings when powered off. Healthcare providers who use these monitors are most at risk.
Check for the CAPNOSTREAM 20P (US) N - ROHS model with part number CS08651-03. The recall includes specific part numbers listed in the record.
Verify that date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
This recall affects CAPNOSTREAM 20P (US) N - ROHS patient monitors with part number CS08651-03. Check the specific part numbers listed in the recall record to see if your monitor is included.
If your monitor resets settings to factory defaults when powered off, check the date/time, nurse call, and alarm settings to ensure they are correct. This is a known issue with the recalled model.
The recall includes specific part numbers listed in the record. Check your monitor's part number against the list provided 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-0023-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0023-2019 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.
