Oridion Medical recalls CAPNOSTREAM 20P patient monitors that may reset date/time and alarm settings to factory defaults when powered off. No immediate action needed but check 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 patient monitors that may reset date/time and alarm settings to factory defaults when powered off. This could cause incorrect patient monitoring if settings are not manually adjusted after power-off.
When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could lead to incorrect patient monitoring if the settings are not manually adjusted after power-off.
Patients using Oridion Medical CAPNOSTREAM 20P monitors with the specified part numbers. Healthcare providers using these monitors are most at risk of incorrect settings.
Check for part numbers listed in the recall: CS08657-01 and the specific serial numbers provided in the description. These monitors were sold with the listed part numbers.
After powering off the monitor, verify that date/time, nurse call, and alarm settings have been manually adjusted to the correct values.
No immediate action is required, but you should check the monitor settings after powering off to ensure they are correct.
The affected part numbers include CS08657-01 and the specific serial numbers listed in the recall description.
This is a low-risk issue as it only affects settings after power-off; no serious injury is expected if settings are manually adjusted.
We’ve drafted a message you can send Oridion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0026-2019 — Oridion Medical Oridion Medical Hello, I own a Oridion Medical that is covered by recall Z-0026-2019 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.
