# FDA recall Z-0920-2022

> **Luminex Corporation** · Class II · device recall initiated 2019-04-22.

## Product

Verigene Processor SP, Model Numbers:  10-0000-07 and 10-0000-07-R

## Reason for recall

Two of three complaints were initiated due to the customers repeatedly obtaining No Call results on the Processor SPs in question.

## Distribution

US:  TX, CT, LA

## Key facts

- **Recall number:** Z-0920-2022
- **Recalling firm:** Luminex Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-04-22
- **Report date:** 2022-04-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northbrook, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0920-2022

## Citation

> AI Analytics. FDA recall Z-0920-2022. Retrieved 2026-08-02 from https://api.ai-analytics.org/recall/Z-0920-2022. Source: US FDA. Licensed CC0.

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