Oridion Medical recalls CAPNOSTREAM 20P bedside monitors with part numbers CS08651-02 and B836141101-B836141120 (and others) due to date/time and alarm settings resetting to factory defaults when powered off.
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 bedside patient monitors because their date/time and nurse call/alarm settings can reset to factory defaults when the monitor is powered off. This could cause incorrect settings to be used during patient monitoring.
When the monitor is powered off, the date/time, nurse call, and alarm settings can reset to factory defaults. This means the monitor might not function correctly when powered on, potentially causing incorrect patient monitoring settings to be used.
Patients using the CAPNOSTREAM 20P bedside monitors with part numbers CS08651-02 and B836141101-B836141120 (and other listed serial numbers) are affected. The risk is low as the issue only affects settings resetting when powered off, not immediate safety hazards.
Check for part number CS08651-02 or serial numbers starting with B836141101 through B836141120 (and other listed serial numbers in the recall list).
Verify that date/time and alarm settings do not reset to factory defaults when the monitor is powered off.
Part number CS08651-02 and serial numbers starting with B836141101 through B836141120 (and other listed serial numbers).
The monitor may reset to factory settings when powered off, potentially causing incorrect date/time or alarm settings to be used during patient monitoring.
Check if your monitor's settings reset to factory defaults when powered off. If so, contact Oridion Medical for guidance.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0022-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0022-2019 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.
