ACON Laboratories Issues a Recall of Non-EUA Authorized “Flowflex™ SARS-CoV-2 Antigen Rapid Test (Self-Testing)” Tests From the U.S. Market

Date: 03/11/2022

Product Type:  Counterfeit, Medical Devices, Unapproved Use

Company Announcement Date: January 09, 2022

FDA Publish Date: January 09, 2022

Product Type: Medical Devices Counterfeit

Reason for Announcement: Unauthorized U.S. distribution-counterfeited product

Company Name: ACON Laboratories, Inc.

Brand Name: Flowflex™

Product Description:  SARS-CoV-2 Antigen Rapid Test (Self-Testing)