Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory defaults when powered off, potentially causing incorrect patient monitoring 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 CAPNOSTREAM 20P bedside patient monitors that may reset to factory default settings when powered off. This could lead to incorrect patient monitoring settings being displayed, which might affect 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 displayed, potentially affecting patient safety if the settings are not properly configured.
Healthcare facilities using the CAPNOSTREAM 20P monitors with part numbers listed in the recall notice. Patients in hospitals or care facilities using these monitors are at risk if settings reset incorrectly.
Check for part numbers listed in the recall notice (e.g., B638137550, B638137552, etc.). The product is a CAPNOSTREAM 20P (INTL) N W/PRINTER model sold internationally.
Verify that the date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
The CAPNOSTREAM 20P monitors may reset to factory default settings when powered off, which could lead to incorrect patient monitoring settings being displayed.
The affected part numbers include B638137550, B638137552, B638137553, and other numbers listed in the recall notice.
No, the recall does not require stopping use. Users should check settings after powering off to ensure they are not reset to factory defaults.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0041-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0041-2019 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.
