# FDA recall Z-0738-2024

> **PHASE SCIENTIFIC INTERNATIONAL LIMITED** · Class II · device recall initiated 2023-10-25.

## Product

INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040

## Reason for recall

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.

## 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.

## Key facts

- **Recall number:** Z-0738-2024
- **Recalling firm:** PHASE SCIENTIFIC INTERNATIONAL LIMITED
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-25
- **Report date:** 2024-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sha Tin, N/A, Hong Kong SAR

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0738-2024

## Citation

> AI Analytics. FDA recall Z-0738-2024. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0738-2024. Source: US FDA. Licensed CC0.

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