---
title: "INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040 — FDA record Z-0738-2024 | Is It on Recall"
description: "COVID-19 rapid antigen at home tests were released with an incorrect expiration date of 05 April 2024 when the correct expiration should be 21 February 2024. Ex"
url: https://isitonrecall.com/recall/fda-device-z-0738-2024-indicaid-covid-19-rapid-antigen-at-home-test-ref-p0040/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040 — FDA record Z-0738-2024

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 Oct 25, 2023. 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**: INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040
- **Reason**: COVID-19 rapid antigen at home tests were released with an incorrect expiration date of 05 April 2024 when the correct expiration should be 21 February 2024. Expired tests could produce invalid or inaccurate results.
- **Classification**: Class II
- **Recalling firm**: PHASE SCIENTIFIC INTERNATIONAL LIMITED
- **Quantity**: 360 Kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0738-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0738-2024%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: 22S0388-R01, Exp: 05-Apr-2024 |

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

## Distribution

US Nationwide distribution including in the states of CA, NY, VT, WA, OH, MD , NJ, PA, MS, NC, AL, MI, MA, DE, GA, TX, OR, MO , WI , ME, IL, VA, CO, NM, NH, LA, KY, DC, MN, MO, FL, AR, MD, TN, UT, WY, SC, WI, CT, KS, SD.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jan 24, 2024
- **Recall initiation date**: Oct 25, 2023
- **Center classification date**: Jan 17, 2024

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-0738-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [PHASE SCIENTIFIC INTERNATIONAL LIMITED records](https://isitonrecall.com/brand/phase-scientific-international-limited/)
