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...
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.
About VEO DIAGNOSTICS, LLC
VEO DIAGNOSTICS, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report