CUE HEALTH INC: Cue Health COVID-19 Test Cartridge REF 2900005 Cue COVID-19
Recall reason: Due to modified test kits being marketed and distributed without FDA Approval, Clearance or Authorization.. Recalled by CUE HEALTH INC. Distribution: U.S. Nationwide distribution.. Classification (Class II — potential health risk). Affected lots/dates: Product code: 2900005 UDI code: N/A Lot Numbers: 30757C 30761G 30760C 30884G 30885G 30762G 30886G 30879C 30882C 30918C 3. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.
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