---
title: "Verigene Processor SP, Models 10-0000-07/10-0000-07R a component of the Verig... — FDA record Z-1092-2022 | Is It on Recall"
description: "Heater within the Verigene System may be outside of established temperature limits for assays which could result in false negative results."
url: https://isitonrecall.com/recall/fda-device-z-1092-2022-verigene-processor-sp-models-10-0000-07-10-0000-07r-a-component-of-the-verigene-system/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Verigene Processor SP, Models 10-0000-07/10-0000-07R a component of the Verigene system — FDA record Z-1092-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 5, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Verigene Processor SP, Models 10-0000-07/10-0000-07R a component of the Verigene system
- **Reason**: Heater within the Verigene System may be outside of established temperature limits for assays which could result in false negative results.
- **Classification**: Class II
- **Recalling firm**: Luminex Corporation
- **Quantity**: 24 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1092-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1092-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Serial Numbers for 10-0000-07: 17340003 19044007 20133004 18128002 18214004 12061048 18191010 13193254 13051068 21029902 16277059 19233005 11250096 14069051 18255003 \*18039010 \*20212006 \*19317004 \*19206009 \*18057008 Serial Numbers added 6.23.22 for 10-0000-07R: 18191010 13051068 14069051 \*12198198 \*12278344 \*14322267 \*12271338 Serial Numbers added 7.14.22 for 10-0000-07R: 18226007 and 16242043 Serial Numbers added 7.14.22 for 10-0000-07: 17062030, 18235008 and 19192006 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US:OH, ME, PA, FL, IL, NE, IN, TX, GA, WA, MI, CO, AZ, OH, KY, CA, VT OUS: None

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
- [Colorado](https://isitonrecall.com/state/colorado/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [Kentucky](https://isitonrecall.com/state/kentucky/)
- [Maine](https://isitonrecall.com/state/maine/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Vermont](https://isitonrecall.com/state/vermont/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: May 25, 2022
- **Recall initiation date**: Apr 5, 2022
- **Center classification date**: May 13, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1092-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Luminex Corporation records](https://isitonrecall.com/brand/luminex-corporation/)