Recall Z-0947-2022— Matrix Medical Network

Name: FDA recall Z-0947-2022
Creator: U.S. Food and Drug Administration
Published: 2022-01-24

Class II · Ongoing

Class II FDA medical device recall by Matrix Medical Network, initiated 2022-01-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Matrix Clinical Solution At-Home COVID-19 Test. Reason: Due to COVID-19 Test not being authorized for home sample collection..

Recalling firm: Matrix Medical Network
Classification: Class II
Status: Ongoing
Initiated: 2022-01-24
Firm location: Scottsdale, AZ, United States

Product description

Matrix Clinical Solution At-Home COVID-19 Test

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.