USA Medical, LLC recalls Diagnostic Kit SARS-cCo V Antigen Rapid Test

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.

Date

2022-05-18

Country

United States

Brand

USA Medical, LLC

Product

Diagnostic Kit SARS-cCo V Antigen Rapid Test

Classification

Class II

Units

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

Category

Drugs & medical

Source

FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

1. Check the product name, strength and lot number against the official notice.
2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

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