Anonymous ID: 0c5902 Dec. 20, 2021, 9:25 a.m. No.15225076   🗄️.is 🔗kun   >>5194

>>15225025

https://www.fda.gov/medical-devices/medical-device-recalls/innova-medical-group-recalls-unauthorized-sars-cov-2-antigen-rapid-qualitative-test-risk-false-test

 

Innova Medical Group Recalls Unauthorized SARS-CoV-2 Antigen Rapid Qualitative Test with Risk of False Test Results

 

likely notabled already but relevant

 

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.