FDAMay 24, 2024device

Cue Health COVID-19 Test Cartridge REF 2900005 Cue COVID-19 Test Cue COVID-19 Test for Home and Over The Counter (OTC)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Due to modified test kits being marketed and distributed without FDA Approval, Clearance or Authorization.

What to do

FDA enforcement status: Ongoing

Brands named

cue healthcue

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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