Normand Informatique Remisol Advance Software: Wrong Results Risk

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Recalling firmNormand InformatiqueNormand Informatique, Sci Git; 57 Grand place; Cs 10451 · Arras CEDEX, N/A N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Normand Informat: Recalls Remisol Advance Software versions 1.6-1.9 because a software issue could cause incorrect results. This affects laboratory systems that manage patient data and workflows.

Why it’s dangerous

A software nonconformity in service settings can cause Remisol to display wrong results. This may lead to incorrect patient data analysis and workflow management.

Who’s affected

Users of Remisol Advance Software versions 1.6-1.9 for laboratory data management systems. Lab technicians and healthcare providers handling patient data are most at risk.

How to tell if you have this one

Check if you have Remisol Advance Software versions 1.6-1.9. The software is used in laboratory systems for data management and patient result workflows.

Brand
Normand Informatique
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Identify your Remisol Advance Software version by checking the software settings or documentation.

✎ GovInfoNow

Questions people ask

What is the specific software version affected?

Remisol Advance Software versions 1.6-1.9.

Why is this software being recalled?

Due to a software nonconformity in service settings that could cause wrong results.

What should I do if I have this software?

The recall record does not specify a remedy, so contact Normand Informatique for assistance.

Take action

Contact Normand Informatique

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

✉️ Open in email

Subject: Recall Z-0235-2018 — Normand Informatique Normand Informatique

Hello,

I own a Normand Informatique that is covered by recall Z-0235-2018 from Normand Informatique.

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-0235-2018 (October 16, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0235-2018 to see it in context.
Plain-language summary written by qwen3:4b on September 14, 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.

Normand Informatique recalls Remisol Advance Software (Driver Architect) Catalog Number B32129 The Remisol Advance Data Manager (Stand alone Data

Lower-risk recall