Migo Trading LLC: Medical Device Recall in 2022 - (Recall #: Z-0421-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

FLOWFLEX SARS-COV-2 Antigen Rapid Test (Self-Testing), 1 Test

Product Classification:

Class II

Date Initiated: November 4, 2021

Date Posted: January 5, 2022

Recall Number: Z-0421-2022

Event ID: 89028

Reason for Recall:

Devices are determined to be inconsistent with the firm's Emergency Use Authorization (EUA). This product has not been authorized for emergency use and the test cannot be determined to be adequately validated for the stated intended use.

Status: Ongoing

Product Quantity: 200,100 units

Code Information:

UDI #: 6921756492427 Lot codes: COV1080232 - Expiration date: 05/13/2023; COV1095004 - Expiration date: 09/03/2023

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated