Skip to content
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.

No adverse-event reports are linked to this device.

Recall history
InitiatedRecall #ClassStatusReasonQuantityLink basis
2026-04-08Z-2168-2026Class IIOpen, ClassifiedComplaints have been received of systems developing loose, missing, or broken internal bolts over time.Distribution: US Nationwide distribution.14837 unitscode info di
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
Similar devices
Select up to two to place side-by-side with this device.