---
title: "Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-090 — FDA record Z-0740-2023 | Is It on Recall"
description: "Reports of an increase in reactive negative controls and false positive results with certain lots of Alinity M Resp-4-Plex AMP kits."
url: https://isitonrecall.com/recall/fda-device-z-0740-2023-abbott-alinity-m-resp-4-plex-amp-kit-part-number-09n79-090/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-090 — FDA record Z-0740-2023

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 Nov 22, 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**: Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-090
- **Reason**: Reports of an increase in reactive negative controls and false positive results with certain lots of Alinity M Resp-4-Plex AMP kits.
- **Classification**: Class II
- **Recalling firm**: Abbott Molecular, Inc.
- **Quantity**: 12116 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0740-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0740-2023%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 | Lot Numbers: 381177, exp 8/24/2023; 525460, exp ; 525766, exp ; 526393, exp ; 526483, exp ; 527142, exp ; 527403, exp ; 527602, exp ; 531612, exp ; |

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

## Distribution

Worldwide

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Dec 28, 2022
- **Recall initiation date**: Nov 22, 2022
- **Center classification date**: Dec 20, 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-0740-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Abbott Molecular, Inc. records](https://isitonrecall.com/brand/abbott-molecular-inc/)