Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory settings when powered off. Affected units have specific part numbers. No remedy provided in recall notice.
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 that may reset their date/time, nurse call, and alarm settings to factory defaults when powered off. This could cause monitoring errors if the settings are critical for 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 monitoring settings being active when the device is turned back on, potentially causing patient safety issues if the settings are critical for patient care.
Healthcare facilities using the recalled CAPNOSTREAM 20P monitors with specific part numbers. Patients in critical care settings where precise monitoring settings are essential are at higher risk.
Check for part numbers listed in the recall notice: B642138114 through B644138291 and other specific numbers in the list. The product is a bedside patient monitor sold internationally.
Verify if the monitor's date/time, nurse call, and alarm settings reset to factory defaults when powered off.
The recall is happening because the monitor may reset its date/time, nurse call, and alarm settings to factory defaults when powered off, which could cause monitoring errors.
Check if your monitor has part numbers listed in the recall notice: B642138114 through B644138291 and other specific numbers in the provided list.
The recall notice does not provide a remedy; the manufacturer has not issued any corrective action.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0037-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0037-2019 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.
