---
title: "Nasopharyngeal sample collection tray for COVID-19 testing, labeled as COVID ... — FDA record Z-1277-2022 | Is It on Recall"
description: "Affected products were assembled off-site by individuals who may not have been properly trained."
url: https://isitonrecall.com/recall/fda-device-z-1277-2022-nasopharyngeal-sample-collection-tray-for-covid-19-testing-labeled-as-covid-test-kit-nonsterile-1843/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Nasopharyngeal sample collection tray for COVID-19 testing, labeled as COVID TEST KIT NONSTERILE 184312, AHCV18A — FDA record Z-1277-2022

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 May 2, 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**: Nasopharyngeal sample collection tray for COVID-19 testing, labeled as COVID TEST KIT NONSTERILE 184312, AHCV18A
- **Reason**: Affected products were assembled off-site by individuals who may not have been properly trained.
- **Classification**: Class I
- **Recalling firm**: American Contract Systems, Inc.
- **Quantity**: 274,400 kits total
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1277-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1277-2022%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 | UDI-DI: 00191072121233 Lots: 721211, 672211, 657211, 994221, 980221, 974221 |

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

## Distribution

US distribution in the state of Minnesota.

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

- [Minnesota](https://isitonrecall.com/state/minnesota/)

## Dates in the source

- **Report date**: Jul 13, 2022
- **Recall initiation date**: May 2, 2022
- **Center classification date**: Jul 1, 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-1277-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [American Contract Systems, Inc. records](https://isitonrecall.com/brand/american-contract-systems-inc/)