Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory settings when powered off. Affected units have specific model numbers and serial ranges. No immediate action is required but users should verify 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 CAPNOSTREAM 20P patient monitors because they may reset to factory settings when powered off. This could cause incorrect alarm or nurse call settings, potentially affecting patient safety if not addressed.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could lead to incorrect alarm triggers or missed patient calls if the settings are not manually adjusted after power-on.
Healthcare professionals using the CAPNOSTREAM 20P bedside monitors with the specific model numbers listed in the recall. Patients are at risk if the monitor settings reset and cause incorrect alarms or missed calls.
Check for model numbers CS051COV or the serial numbers ME30160001 through ME30160016 on the device. The product was sold with the specific model and serial numbers listed in the recall.
After powering on the monitor, verify that the date/time, nurse call, and alarm settings are correct and have not reset to factory defaults.
No, the recall does not require stopping use. You can continue using the monitor but should check settings after power-on.
The affected model numbers are CS051COV with serial numbers ME30160001 through ME30160016.
The recall does not provide a fix. Users must manually verify settings after each power cycle.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0055-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0055-2019 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.
