Loveland, OH, United States
VEO DIAGNOSTICS, LLC recalls
1 recall recorded since 2018, most recently on 5 November 2020. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 5 November 2020
- Terminated
- 16 April 2021
- Reason
- Emergency Use Authorization (EUA) removed from list of COVID-19 antibody tests
- Distribution
- US Nationwide distribution including in the states of IA, PA, WA.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0510-2021
- 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
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.