Medical device recalls Moderate risk

Matrix Medical Network recalls Matrix Clinical Solution At-Home COVID-19 Test

Recall date
January 24, 2022
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0947-2022
FDA classification
Class II
Brand / firm
Matrix Medical Network
Sold / distributed
U.S.: AL, AZ, CA, CO, CT, DC, DE, FL, GA, LA, MA, MD, MI, MN, NH, NJ, NY, OH, OK, PA, TN, TX, UT, VA, and WV. O.U.S.: N/A

Why it was recalled

Due to COVID-19 Test not being authorized for home sample collection.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Matrix Clinical Solution At-Home COVID-19 Test

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