---
title: "FLOWFLEX SARS-COV-2 Antigen Rapid Test (Self-Testing), 1 Test — FDA record Z-0421-2022 | Is It on Recall"
description: "Devices are determined to be inconsistent with the firm's Emergency Use Authorization (EUA). This product has not been authorized for emergency use and the test"
url: https://isitonrecall.com/recall/fda-device-z-0421-2022-flowflex-sars-cov-2-antigen-rapid-test-self-testing-1-test/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# FLOWFLEX SARS-COV-2 Antigen Rapid Test (Self-Testing), 1 Test — FDA record Z-0421-2022

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 Nov 4, 2021. 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**: FLOWFLEX SARS-COV-2 Antigen Rapid Test (Self-Testing), 1 Test
- **Reason**: Devices are determined to be inconsistent with the firm's Emergency Use Authorization (EUA). This product has not been authorized for emergency use and the test cannot be determined to be adequately validated for the stated intended use.
- **Classification**: Class II
- **Recalling firm**: Migo Trading LLC
- **Quantity**: 200,100 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0421-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0421-2022%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 #: 6921756492427 Lot codes: COV1080232 - Expiration date: 05/13/2023; COV1095004 - Expiration date: 09/03/2023 |

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

## Distribution

NY

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

- [New York](https://isitonrecall.com/state/new-york/)

## Dates in the source

- **Report date**: Jan 5, 2022
- **Recall initiation date**: Nov 4, 2021
- **Center classification date**: Dec 27, 2021

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-0421-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Migo Trading LLC records](https://isitonrecall.com/brand/migo-trading-llc/)