North American Diagnostics Recalls Oral Rapid SARS-CoV-2 Rapid Antigen Test Kits That Are Not Authorized, Cleared, or Approved by the FDA
Predatory companies often take advantage of the desperation of consumers and the market when they believe there is profit to be made. This often comes at a cost to others. The FDA has identified this as a the most serious type of recall: Class I that recalls that states the use of these devices may cause serious injuries or death.
In a time when our health is of utmost importance, it is imperative to do your research and stay informed to protect yourself and your loved ones.
The test being recalled is Oral Rapid SARS-CoV-2 Rapid Antigen Test Kit. Other names and more information can be found by visiting the following link:
https://www.fda.gov/medical-devices/medical-device-recalls/north-american-diagnostics-recalls-oral-rapid-sars-cov-2-rapid-antigen-test-kits-are-not-authorized
