Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

ACCEL ELISA COVID-19 for the detection of total antibodies to Recalled by VEO DIAGNOSTICS, LLC Due to Emergency Use Authorization (EUA) removed from list of...

Date: November 5, 2020
Company: VEO DIAGNOSTICS, LLC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact VEO DIAGNOSTICS, LLC directly.

Affected Products

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

Quantity: 15 kits

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About VEO DIAGNOSTICS, LLC

VEO DIAGNOSTICS, LLC has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report