Oridion CAPNOSTREAM 20P Bedside Monitor: Settings Reset Risk

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Contact the company & request your remedy

Recalling firmOridion Medical 1987 Ltd.Har Hotzvim Industrial Park Box 45025, Har Hotzvim Industrial Park · Jerusalem, N/A

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Oridion's CAPNOSTREAM 20P bedside patient monitors may reset to factory settings when powered off. This could cause settings to be incorrect after the monitor is turned off. No action is needed if the monitor's settings appear correct.

Why it’s dangerous

When the monitor is powered off, the date/time, nurse call, and alarm settings may reset to factory defaults. This could cause incorrect settings to be used after the monitor is turned back on, but the risk is low as the reset only affects settings, not patient safety.

Who’s affected

Patients using Oridion CAPNOSTREAM 20P bedside monitors with the listed part numbers. The risk is low as the reset only affects settings, not patient safety.

How to tell if you have this one

Check if your monitor has part numbers listed in the recall (B819140007 through B851165300). The product is a bedside patient monitor sold in the US.

Brand
Oridion
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check monitor settings
Verify that date/time, nurse call, and alarm settings appear correct after the monitor is powered on.

✎ GovInfoNow

Questions people ask

Do I need to do anything with my monitor?

No action is needed if the monitor's settings appear correct after being powered on.

What part numbers are affected?

The affected units have specific part numbers listed in the recall (B819140007 through B851165300).

Could this cause injury?

The reset only affects settings, not patient safety. The risk is low as the reset does not cause immediate harm.

Take action

Contact Oridion

We’ve drafted a message you can send Oridion to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0025-2019 — Oridion Oridion

Hello,

I own a Oridion that is covered by recall Z-0025-2019 from Oridion.

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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Where this comes from

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.

Official source: FDA Recall #Z-0025-2019 (July 31, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0025-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Oridion Medical 1987 Ltd. recalls CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-02

Lower-risk recall