Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset to factory defaults when powered off. Affected units have specific part numbers. No immediate action needed as settings reset is not a safety hazard.
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 their CAPNOSTREAM 20P bedside patient monitors because settings may reset to factory defaults when the monitor is powered off. This issue does not pose a safety risk to patients or users.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could cause confusion in monitoring settings but does not pose a safety risk to patients or users.
Healthcare facilities using the CAPNOSTREAM 20P monitors with specific part numbers listed in the recall. Patients and staff are not at risk as the reset does not affect patient safety.
Check if your monitor has part numbers listed in the recall (e.g., PA12170508, PA14170801, PA23172302, etc.). The product is a bedside patient monitor sold internationally.
Verify if your monitor resets to factory defaults when powered off by checking date/time, nurse call, and alarm settings after powering off and on.
No, the reset of settings does not pose a safety risk to patients or users. The recall is for informational purposes only.
The affected part numbers are listed in the recall (e.g., PA12170508, PA14170801, PA23172302, etc.).
No immediate action is needed. The reset is not a safety hazard, but you can check if your monitor resets settings when powered off.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0039-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0039-2019 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.
