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DIGITAL DIAGNOSTICS SYSTEM

Hologic, Inc. · Model ASSEMBLY, REVIEW STATION COMPUTER · UDI-DI 15420045517097

QYV Prescription
1
510(k) clearances
5
Adverse events
1
Recalls
1
Facilities

Description

Computer to operate the Genius™ Review Station.

Recalls

DateFirmReason
2026-03-23Hologic, IncIt was identified that certain devices were being operated outside the validated and FDA-cleared display configuration due to user modification of the manufacturer-installed settin

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.