Dna-reagents, Neisseria
Hologic, Inc.'s record for this product code
MDR events75All time
Recalls0All time
510(k) clearances2All time
Recent MDR events
75 adverse event reports on file
- APTIMA COMBO 2 ASSAYJul 21, 2026Injury2024800-2026-00046
- APTIMA COMBO 2 ASSAYJul 17, 2026Injury2024800-2026-00043
- APTIMA URINE SPECIMEN COLLECTION KIT FOR MALE AND FEMALE URINE SPECIMENSJun 16, 2026Injury2024800-2026-00034
- APTIMA COMBO 2 ASSAYJun 3, 2026Injury2024800-2026-00027
- APTIMA COMBO 2 ASSAYMay 27, 2026Injury2024800-2026-00024
- APTIMA COMBO 2 ASSAYMay 8, 2026Injury2024800-2026-00021
- APTIMA COMBO 2 ASSAYApr 13, 2026Injury2024800-2026-00019
- APTIMA UNISEX SWAB SPECIMEN COLLECTION KITFeb 25, 2026Malfunction2024800-2026-00006
- APTIMA COMBO 2 ASSAYFeb 4, 2026Injury2024800-2026-00004
- APTIMA COMBO 2 ASSAYDec 16, 2025Injury2024800-2025-00076
Recalls
0 recall events for this product code
No recalls on file for Hologic, Inc. under this product code.
510(k) clearances
2 clearances for this product code