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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

81 linked reportsInjury 43Malfunction 38
25792019-01: 0 reports for this device; peer average 6/device2019-02: 4 reports for this device; peer average 2.5/device2019-03: 3 reports for this device; peer average 4.5/device2019-04: 6 reports for this device; peer average 7/device2019-05: 5 reports for this device; peer average 4/device2019-06: 3 reports for this device; peer average 4/device2019-07: 0 reports for this device; peer average 3.5/device2019-08: 3 reports for this device; peer average 4.5/device2019-09: 0 reports for this device; peer average 3/device2019-11: 0 reports for this device; peer average 9/device2019-12: 0 reports for this device; peer average 3/device2020-01: 3 reports for this device; peer average 3/device2020-02: 0 reports for this device; peer average 3.67/device2020-09: 0 reports for this device; peer average 3/device2021-02: 0 reports for this device; peer average 1/device2021-05: 0 reports for this device; peer average 3/device2021-09: 0 reports for this device; peer average 3.5/device2021-11: 0 reports for this device; peer average 2/device2022-01: 2 reports for this device; peer average 2/device2022-09: 0 reports for this device; peer average 1/device2022-10: 1 reports for this device; peer average 1/device2023-01: 0 reports for this device; peer average 4/device2023-02: 3 reports for this device; peer average 2.5/device2023-06: 3 reports for this device; peer average 3/device2024-02: 0 reports for this device; peer average 3/device2024-04: 3 reports for this device; peer average 3/device2024-08: 3 reports for this device; peer average 3/device2024-09: 0 reports for this device; peer average 1/device2025-02: 2 reports for this device; peer average 2/device2025-04: 0 reports for this device; peer average 2.5/device2025-08: 2 reports for this device; peer average 2/device2025-09: 0 reports for this device; peer average 6/device2025-10: 9 reports for this device; peer average 9/device2025-11: 3 reports for this device; peer average 4.5/device2025-12: 0 reports for this device; peer average 3/device2026-01: 3 reports for this device; peer average 4/device2026-02: 6 reports for this device; peer average 6/device2026-03: 8 reports for this device; peer average 5.5/device2026-04: 0 reports for this device; peer average 2/device2026-05: 2 reports for this device; peer average 2/device2026-06: 4 reports for this device; peer average 3/device0102030405060708091112010209020509110109100102060204080902040809101112010203040506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0106
2019-0242.5
2019-0334.5
2019-0467
2019-0554
2019-0634
2019-0703.5
2019-0834.5
2019-0903
2019-1109
2019-1203
2020-0133
2020-0203.67
2020-0903
2021-0201
2021-0503
2021-0903.5
2021-1102
2022-0122
2022-0901
2022-1011
2023-0104
2023-0232.5
2023-0633
2024-0203
2024-0433
2024-0833
2024-0901
2025-0222
2025-0402.5
2025-0822
2025-0906
2025-1099
2025-1134.5
2025-1203
2026-0134
2026-0266
2026-0385.5
2026-0402
2026-0522
2026-0643
This device (reports/month)Average device in IZH (reports/device/month)
Failure-mode summaryAI-generated

40 linked report narratives available — no AI summary generated yet.

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-06-153005496266-2026-00156InjuryAvailablecatalog number
2026-06-123005496266-2026-00148InjuryAvailablecatalog number
2026-05-053005496266-2026-00096InjuryAvailablecatalog number
2026-03-253005496266-2026-00063InjuryAvailablecatalog number
2026-03-193005496266-2026-00056MalfunctionAvailablecatalog number
2026-03-133005496266-2026-00053MalfunctionAvailablecatalog number
2026-02-203005496266-2026-00034InjuryAvailablecatalog number
2026-02-063005496266-2026-00017InjuryAvailablecatalog number
2026-01-153005496266-2026-00010InjuryAvailablecatalog number
2025-11-193005496266-2025-00098InjuryAvailablecatalog number
2025-10-203005496266-2025-00075InjuryAvailablecatalog number
2025-10-073005496266-2025-00066InjuryAvailablecatalog number
2025-10-073005496266-2025-00068InjuryAvailablecatalog number
2025-08-073005496266-2025-00045InjuryAvailablecatalog number
2025-02-051220984-2025-00010InjuryAvailablecatalog number

Showing the most recent 31 of 81 linked reports.

Showing 115 of 31
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2025-11-04OAIOfficial action indicatedHologic, Inc3
2025-11-04OAIOfficial action indicatedHologic, Inc3
2024-12-18WLWarning LetterHologic, Inc
2024-12-18WLWarning LetterHologic, Inc
2024-09-24OAIOfficial action indicatedHologic, Inc5
2024-09-24OAIOfficial action indicatedHologic, Inc5
2024-09-12VAIVoluntary action indicatedHologic Surgical Products Costa Rica, S.R.L.0
2024-08-13NAINo action indicatedHologic, Inc.0
2024-08-13NAINo action indicatedHologic, Inc.0
2022-12-14NAINo action indicatedBolder Surgical, LLC0
2022-10-14OAIOfficial action indicatedHologic, Inc.4
2022-10-14OAIOfficial action indicatedHologic, Inc.4
2022-08-03VAIVoluntary action indicatedHealth Beacons, Inc.1
2020-02-25NAINo action indicatedHealth Beacons, Inc.0
2018-12-10NAINo action indicatedHologic, Inc.0
2018-12-10NAINo action indicatedHologic, Inc.0
2018-02-27NAINo action indicatedGynesonics, Inc.0
2017-11-30NAINo action indicatedHologic, Inc0
2017-11-30NAINo action indicatedHologic, Inc0
2017-11-27VAIVoluntary action indicatedBolder Surgical, LLC6
2017-10-25NAINo action indicatedHologic, Inc.0
2017-10-25NAINo action indicatedHologic, Inc.0
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