Oridion Medical recalls CAPNOSTREAM 20 bedside monitors that may reset to factory settings when powered off, potentially causing incorrect patient monitoring.
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 20 bedside patient monitors that may reset to factory settings when powered off. This could lead to incorrect patient monitoring settings, which might delay critical medical responses if the monitor is used for vital signs.
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 active, potentially delaying critical medical responses if the monitor is used for vital signs.
Healthcare professionals using the CAPNOSTREAM 20 bedside monitors for patient monitoring. Patients with critical medical conditions are most at risk if the monitor settings reset and cause incorrect readings.
The CAPNOSTREAM 20 (INTL) N W/PRINTER model with part number CS08658. These units were sold with serial numbers starting with B200001028 through B428136466.
Verify that the date/time, nurse call, and alarm settings are not reset to factory defaults after powering off the monitor.
The monitor may reset to factory settings when powered off, potentially causing incorrect patient monitoring settings.
Check the serial number on your monitor; affected units have serial numbers starting with B200001028 through B428136466.
You can check if settings reset by powering off the monitor and verifying the date/time, nurse call, and alarm settings. No action is required if settings remain correct.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0040-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0040-2019 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.
