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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.

5 linked reportsInjury 5
13452019-06: 0 reports for this device; peer average 1/device2019-07: 0 reports for this device; peer average 1/device2019-08: 0 reports for this device; peer average 1/device2019-09: 0 reports for this device; peer average 1/device2020-06: 0 reports for this device; peer average 1/device2020-10: 0 reports for this device; peer average 1/device2021-05: 0 reports for this device; peer average 2/device2022-07: 0 reports for this device; peer average 1/device2023-02: 0 reports for this device; peer average 1/device2023-12: 0 reports for this device; peer average 1/device2024-04: 0 reports for this device; peer average 1/device2025-08: 0 reports for this device; peer average 5/device2025-09: 0 reports for this device; peer average 2/device2025-10: 1 reports for this device; peer average 4.5/device2025-11: 1 reports for this device; peer average 2.5/device2025-12: 0 reports for this device; peer average 5/device2026-01: 0 reports for this device; peer average 1/device2026-02: 1 reports for this device; peer average 3/device2026-03: 1 reports for this device; peer average 3/device2026-04: 0 reports for this device; peer average 1/device2026-05: 0 reports for this device; peer average 2/device2026-06: 1 reports for this device; peer average 1/device06070809061005070212040809101112010203040506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0601
2019-0701
2019-0801
2019-0901
2020-0601
2020-1001
2021-0502
2022-0701
2023-0201
2023-1201
2024-0401
2025-0805
2025-0902
2025-1014.5
2025-1112.5
2025-1205
2026-0101
2026-0213
2026-0313
2026-0401
2026-0502
2026-0611
This device (reports/month)Average device in HDF (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-06-153013111692-2026-18696InjuryAvailableexact di
2026-03-303013111692-2026-10427InjuryAvailableexact di
2026-02-123013111692-2026-05803InjuryAvailableexact di
2025-11-123013111692-2025-32151InjuryAvailableexact di
2025-10-273013111692-2025-30629InjuryAvailableexact di
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2023-12-05VAIVoluntary action indicatedInstrumed International Inc5
2022-06-28VAIVoluntary action indicatedAvalign Integrated Medical Solutions, Inc.3
2019-11-20VAIVoluntary action indicatedInstrumed International Inc2
2018-10-25NAINo action indicatedInstrumed GmbH0
2016-11-30NAINo action indicatedInstrumed International Inc0
2015-09-22NAINo action indicatedMillennium Surgical Corp0
2015-01-29NAINo action indicatedInstrumed GmbH0
2014-03-28WLWarning LetterInstrumed GmbH
2013-08-20VAIVoluntary action indicatedInstrumed International Inc17
2013-08-01OAIOfficial action indicatedInstrumed GmbH0
2013-04-24VAIVoluntary action indicatedAvalign Integrated Medical Solutions, Inc.4
2011-02-28NAINo action indicatedInstrumed International Inc0
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