---
title: "Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test — FDA record Z-1045-2022 | Is It on Recall"
description: "Firm distributed tests which have not been cleared or authorized for marketing or distribution in the United States."
url: https://isitonrecall.com/recall/fda-device-z-1045-2022-joysbio-sars-cov-2-antigen-rapid-test-kit-colloidal-gold-covid-19-test/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test — FDA record Z-1045-2022

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 9, 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**: Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test
- **Reason**: Firm distributed tests which have not been cleared or authorized for marketing or distribution in the United States.
- **Classification**: Class I
- **Recalling firm**: Woodside Acquisitions Inc.
- **Quantity**: 17,000 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1045-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1045-2022%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 | All lots |

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

## Distribution

US distributions to states of: AL and GA.

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

- [Alabama](https://isitonrecall.com/state/alabama/)
- [Georgia](https://isitonrecall.com/state/georgia/)

## Dates in the source

- **Report date**: May 18, 2022
- **Recall initiation date**: Apr 9, 2022
- **Center classification date**: May 12, 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-1045-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Woodside Acquisitions Inc. records](https://isitonrecall.com/brand/woodside-acquisitions-inc/)