company
Hologic, Inc
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-05-20Hologic, Inc — Class II recall: 3DIMENSIONS MAMMOGRAPHY SYSTEM; Model Numbers: 3DM-SYS-INTL2D, 3DM-SYS-INTL2D-MO…
- fda_recall · device_recall2026-05-20Hologic, Inc — Class II recall: SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-…
- fda_recall · device_recall2026-05-06Hologic, Inc — Class II recall: Brand Name: Genius" Review Station Product Name: Genius" Review Station Display…
Frequently asked questions
- How many FDA warning letters has Hologic, Inc received?
- Argus HQ has not recorded an FDA warning letter for Hologic, Inc in our current dataset.
- What FDA recalls has Hologic, Inc issued?
- Argus HQ has recorded 3 FDA recalls tied to Hologic, Inc.
- Is Hologic, Inc FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 3 recalls, and 0 approval records for Hologic, Inc. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.