Oridion Medical recalls CAPNOSTREAM 20P bedside monitors that may reset date/time and alarm settings to factory defaults when powered off. Affected units have specific part numbers listed in the 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 bedside patient monitors because they may reset date/time and alarm settings to factory defaults when the monitor is powered off. This could lead to incorrect patient monitoring settings being active.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory default values. This could cause incorrect patient monitoring settings to be active, potentially leading to missed alarms or incorrect patient data.
Patients using the CAPNOSTREAM 20P bedside monitors with the specific part numbers listed in the recall notice. Healthcare providers who use these monitors for patient monitoring are most at risk.
Check the product's part number on the device or packaging. Affected units include specific part numbers listed in the recall notice, such as CS08657-03 and PA10170221 through PA36173715.
Look for the part number on the device or packaging to confirm if it's affected.
The monitor may reset date/time and alarm settings to factory defaults when powered off, which could lead to incorrect patient monitoring settings.
Check the part number on the device or packaging. Affected units have specific part numbers listed in the recall notice, such as CS08657-03 and PA10170221 through PA36173715.
The recall does not specify a remedy, so no action is required beyond checking the part number.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0027-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0027-2019 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.
