FDAClass IIJanuary 24, 2024

INDICAID COVID-19 Rapid Antigen At-Home Test recall

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

Why was INDICAID COVID-19 Rapid Antigen At-Home Test recalled?

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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040
Recalling firm
PHASE SCIENTIFIC INTERNATIONAL LIMITED
Quantity
360 Kits
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.
Recall date
January 24, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls