# FDA recall Z-0158-2020

> **Vital Scientific N.V.** · Class II · device recall initiated 2012-01-10.

## Product

Selectra ProS Analyzer, Catalog # 6003-600/UDI # 03661540600418    Product Usage:  :clinical chemistry system intended for use in clinical laboratories.

## Reason for recall

The action was initiated due  power supply failure. During  a power supply failure the instruments malfunctions and no patient results are produced.

## Distribution

US Nationwide in the states of NY, and UT

## Key facts

- **Recall number:** Z-0158-2020
- **Recalling firm:** Vital Scientific N.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2012-01-10
- **Report date:** 2019-10-23
- **Termination date:** 2024-04-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dieren, N/A, Netherlands

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0158-2020

## Citation

> AI Analytics. FDA recall Z-0158-2020. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-0158-2020. Source: US FDA. Licensed CC0.

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