FDAMarch 1, 2021device
Cellex qSARS-Cov-2 Antigen Rapid Test, 25 tests/box, submitted as EUA202955 "declined to issue"
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The kit does not have an emergency use authorization (EUA).
What to do
FDA enforcement status: Ongoing
Brands named
cellex
Recall history
No related federal recalls on record for this brand yet.
Own something like this?
AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.
Start free — 200 items, no card →