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Aptima®

Hologic, Inc. · Model KIT,HPV,APTIMA, CALIBRATORS, IVD · UDI-DI 15420045500075

OYB Prescription
0
510(k) clearances
42
Adverse events
1
Recalls
1
Facilities

Description

Aptima® HPV Assay Calibrators Kit.

Recalls

DateFirmReason
2026-02-18Hologic, Inc.Due to product exhibiting potential to generate either invalid or false negative results.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.