PHASE SCIENTIFIC recalls INDICAID COVID-19 Rapid Antigen Tests with wrong expiration date (05 Apr 2024 vs correct 21 Feb 2024). Expired tests may give invalid results.
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.
PHASE SCIENTIFIC is recalling INDICAID COVID-19 Rapid Antigen At-Home Tests that were shipped with an incorrect expiration date. Using these expired tests could lead to inaccurate results, which might affect your ability to correctly detect COVID-19.
The tests were shipped with an expiration date of 05 April 2024 instead of the correct 21 February 2024. If used after the correct expiration date, the tests may produce invalid or inaccurate results, meaning they could fail to detect COVID-19 infection.
Anyone who purchased the INDICAID COVID-19 Rapid Antigen At-Home Test with the incorrect expiration date of 05 April 2024. People who use these tests for regular home testing are most at risk of getting inaccurate results.
Check for the product name 'INDICAID COVID-19 Rapid Antigen At-Home Test' with reference number P0040 and expiration date 05-Apr-2024 on the packaging.
Verify the expiration date on the test packaging is 05 April 2024 (not 21 February 2024).
The tests were shipped with an incorrect expiration date of 05 April 2024 instead of the correct 21 February 2024, which could lead to inaccurate results.
Check the expiration date on the packaging. If it shows 05 April 2024, it is part of the recall and may give invalid results.
The official recall does not provide a fix; users should check the expiration date and avoid using tests with the incorrect date.
We’ve drafted a message you can send PHASE SCIENTIFIC to request your refund or repair — edit it as you like.
Subject: Recall Z-0738-2024 — PHASE SCIENTIFIC PHASE SCIENTIFIC Hello, I own a PHASE SCIENTIFIC that is covered by recall Z-0738-2024 from PHASE SCIENTIFIC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
