WSB-TV

Recall alert: Jiangsu Well Biotech recalls COVID-19 Ag rapid test devices lacking FDA authorization

WASHINGTON — Jiangsu Well Biotech Co. Ltd. on Wednesday recalled its COVID-19 Ag Rapid Test devices because they were distributed to U.S. customers without authorization, clearance or approval from ...
Healio

FDA approves at-home rapid test for influenza, COVID-19

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. The FDA issued an emergency use authorization for CorDx ...
Channel NewsAsia Singapore

Covid-19 antigen rapid test kits in Singapore not affected by US FDA advisory: HSA

Samples of antigen rapid test kits: (from left) Acon Flowflex Sars-CoV-2 Antigen Rapid Test (Self-Testing) and SD Biosensor Standard Q Covid-19 Ag Home Test. SINGAPORE — The supplies in Singapore of ...
FierceBiotech

QuidelOrtho's rapid antigen COVID test is first to receive regular clearance from the FDA

Since the start of the pandemic, the FDA has issued emergency use authorizations to a whopping 444 diagnostic tests and sample collection devices to detect the COVID-19 virus. In recent months, ...
Healthline

BinaxNOW COVID-19 Test Review: Cost, Accuracy, How It Works

The BinaxNOW COVID-19 Antigen Self-Test is an FDA-approved at-home test kit. It can detect active infections with SARS-CoV-2, the virus that causes COVID-19, in ...
The American Journal of Managed Care

Nasal Swab Test Can Predict COVID-19 Severity Through Autoantibody Analysis

Severity of a COVID-19 illness could be determined by examining autoantibodies in the nasal cavity, allowing more personalized treatment protocols. Severe COVID-19 can be life-threatening for patients ...