FDA recall record

USA Medical Diagnostic Kit SARS-cCo V Antigen Rapid Test recall — FDA Z-1050-2022

COVID-19/SARS-CoV-2 Antigen Tests did not receive FDA Emergency Use Authorization, nor were the tests cleared or approved to be commercially distributed.

Class IIclassification
Z-1050-2022official record ID
May 18, 2022report date

Recall record at a glance

Official recordZ-1050-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmUSA Medical, LLC
Report dateMay 18, 2022
Recall initiation dateApr 4, 2022
Quantity2055 kits
LocationGrapevine, TX, United States

Official product description

Diagnostic Kit SARS-cCo V Antigen Rapid Test

Why the product was recalled

COVID-19/SARS-CoV-2 Antigen Tests did not receive FDA Emergency Use Authorization, nor were the tests cleared or approved to be commercially distributed.

Distribution information

U.S. Nationwide distribution in the states of CA, FL, IN, MD, MO, NJ, OK, and TN.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.