VEO DIAGNOSTICS, LLC recalls ACCEL ELISA COVID-19 for the detection of total antibodies to SARS-CoV-2 Catalog AE301U Kit lots: PXCOV073020, PXCOV

Recalled December 9, 2020 · FDA recall Z-0510-2021 · VEO DIAGNOSTICS

Hazard

Emergency Use Authorization (EUA) removed from list of COVID-19 antibody tests · FDA Class II

Units

15 kits

Sold at

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

Description

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

Product

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

Manufacturer(s)

VEO DIAGNOSTICS, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →