PHASE SCIENTIFIC INTERNATIONAL LIMITED: Medical Device Recall in 2024 - (Recall #: Z-0738-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: October 25, 2023

Date Posted: January 24, 2024

Recall Number: Z-0738-2024

Event ID: 93626

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.

Status: Ongoing

Product Quantity: 360 Kits

Code Information:

Lot: 22S0388-R01, Exp: 05-Apr-2024

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated