# FDA recall Z-2743-2020

> **Normand-Info S.A.S.U.** · Class II · device recall initiated 2020-04-30.

## Product

Remisol Advance running Software Version 1.12    The Normand Info Remisol Advance Data Manager collects and manages data and workflow for 128 connections (Beckman Coulter Instruments, automations, LIS &). It can also be connected to a host system.

## Reason for recall

Results from repeated run for WBC (White Bloodcell Count), UWBC (Urine Whit Bloodcell Count) and PLT (Platelets) are deleted in RADV. Use may lead to erroneous results.

## Distribution

Worldwide distribution: US (nationwide) including states of: CA, GA, IL, IN, KS, MI, MO, NY, NC, OH, PA, SD, TN, VA, and WV;  and countries of: Bahrain, Belgium, Canada, China, Czech Republic, France, Germany, Hong Kong, Israel, Malaysia, Netherlands, Switzerland, Taiwan,Turkey, and United Kingdom.

## Key facts

- **Recall number:** Z-2743-2020
- **Recalling firm:** Normand-Info S.A.S.U.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-30
- **Report date:** 2020-08-12
- **Termination date:** 2022-02-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arras CEDEX, France

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2743-2020

## Citation

> AI Analytics. FDA recall Z-2743-2020. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-2743-2020. Source: US FDA. Licensed CC0.

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