Matrix Clinical Solution At-Home COVID-19 Test
Reported: April 27, 2022 Initiated: January 24, 2022 #Z-0947-2022
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.
Details
- Recalling Firm
- Matrix Medical Network
- Units Affected
- 3,226 kits
- Distribution
- 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
- Location
- Scottsdale, AZ
Frequently Asked Questions
What product was recalled? ▼
Matrix Clinical Solution At-Home COVID-19 Test. Recalled by Matrix Medical Network. Units affected: 3,226 kits.
Why was this product recalled? ▼
Due to COVID-19 Test not being authorized for home sample collection.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 27, 2022. Severity: Moderate. Recall number: Z-0947-2022.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11