https://templarpharma.com/fda-warns-against-use-of-renuvion-j-plasma-device-for-certain-aesthetic-procedures-fda-safety-communication/

Date: 03/14/2022

Product type:  Medical Device

Product Names:

•  COVID-19 Antigen Test (Saliva)
• COVID-19 Antigen Test (Nasal)
• COVID-19 IgG/IgM Antibody Test

Product code:

• See Recall Database Entry

Distribution Dates: June 1, 2020 to July 21, 2021

Devices Recalled in the U.S.: 164,250

Date Initiated by Firm: January 13, 2022

USA-FDA link: https://www.fda.gov/medical-devices/medical-device-recalls/lusys-laboratories-inc-recalls-covid-19-antigen-tests-nasalsaliva-and-covid-19-iggigm-antibody-tests