VEO DIAGNOSTICS, LLC: Medical Device Recall in 2020 - (Recall #: Z-0510-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

ACCEL ELISA COVID-19 for the detection of total antibodies to SARS-CoV-2 Catalog AE301U Kit lots: PXCOV073020, PXCOV081220 Expiration dates: January 18, 2021 and January 26, 2021

Product Classification:

Class II

Date Initiated: November 5, 2020

Date Posted: December 9, 2020

Recall Number: Z-0510-2021

Event ID: 86798

Reason for Recall:

Emergency Use Authorization (EUA) removed from list of COVID-19 antibody tests

Status: Terminated

Product Quantity: 15 kits

Code Information:

Kit lots: PXCOV073020, PXCOV081220 Expiration dates: January 18, 2021 and January 26, 2021

Distribution Pattern:

US Nationwide distribution including in the states of IA, PA, WA.

Voluntary or Mandated:

Voluntary: Firm initiated