FDAClass IFebruary 9, 2022

CovClear COVID-19 Rapid Antigen Test recall

CovClear COVID-19 Rapid Antigen Test, ATG 900-031

Why was CovClear COVID-19 Rapid Antigen Test recalled?

COVID test kits were offered for sale and distributed to consumers in the United States without marketing approval, clearance, or authorization from FDA.

What should I do if I have this product?

Review the official FDA enforcement record for current 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?

All lots

Product
CovClear COVID-19 Rapid Antigen Test, ATG 900-031
Recalling firm
Empowered Diagnostics LLC
Quantity
284,575 units
Distribution
US Nationwide Distribution
Recall date
February 9, 2022
Classification
Class I
Status
Completed
Agency
FDA (device)
Open FDA enforcement record Latest recalls