SARS-CoV-2 Antigen Test (USA Medical) – Unauthorized Distribution (2022)

Check Your Product

According to the U.S. Food and Drug Administration (FDA)

Reason for Recall

As stated by FDA

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.

Recommended Action

Per FDA guidance

On 04/04/2022, US Medical LLC sent an "URGENT MEDICAL DEVICE RECALL" Letter via certified US Postal informing customers that USA Medical LLC is voluntarily recalling all COVID-19 Rapid test, labeled as Diagnostic Kit COVID-19 Antigen Rapid Test and may have included components labeled DiaTrust COVID-19 Ag Rapid Test. These COVID-19 antigen tests distributed by USA Medical have not received FDA Emergency Use Authorization, nor have these tests been cleared or approved by FDA for commercial distribution. Customers are instructed to: 1. Discontinue use, discard, or return the product back to USA Medical using the enclosed pre-paid Fed Ex return shipping label. 2. If you have further distributed these products, immediately notify these customers and provide them with the recall notification. 3. Please fill out and return that attached Acknowledgement and Receipt Form. Any further questions or require assistance: Contact Monday thru Friday 9:00am to 5:00pm Central time at 817-416-9900