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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.

6 linked reportsInjury 6
12232019-02: 0 reports for this device; peer average 1/device2019-03: 0 reports for this device; peer average 2/device2019-04: 0 reports for this device; peer average 2/device2019-07: 0 reports for this device; peer average 1/device2019-08: 0 reports for this device; peer average 1/device2019-10: 0 reports for this device; peer average 3/device2019-12: 0 reports for this device; peer average 2/device2021-05: 0 reports for this device; peer average 3/device2021-07: 0 reports for this device; peer average 3/device2021-11: 0 reports for this device; peer average 1/device2021-12: 0 reports for this device; peer average 1/device2022-07: 3 reports for this device; peer average 3/device2022-09: 0 reports for this device; peer average 2/device2023-05: 0 reports for this device; peer average 3/device2023-06: 0 reports for this device; peer average 1/device2023-08: 0 reports for this device; peer average 1/device2023-09: 0 reports for this device; peer average 1/device2023-10: 0 reports for this device; peer average 2/device2023-11: 0 reports for this device; peer average 2/device2024-01: 0 reports for this device; peer average 1/device2024-02: 0 reports for this device; peer average 2/device2024-04: 0 reports for this device; peer average 2/device2024-06: 0 reports for this device; peer average 1/device2024-07: 0 reports for this device; peer average 1/device2024-08: 0 reports for this device; peer average 1/device2024-09: 0 reports for this device; peer average 2/device2024-10: 0 reports for this device; peer average 1/device2025-01: 0 reports for this device; peer average 1/device2025-03: 0 reports for this device; peer average 2/device2025-05: 0 reports for this device; peer average 1/device2025-08: 0 reports for this device; peer average 2/device2025-10: 0 reports for this device; peer average 1/device2025-11: 0 reports for this device; peer average 1.5/device2026-01: 0 reports for this device; peer average 1/device2026-02: 1 reports for this device; peer average 1.5/device2026-03: 0 reports for this device; peer average 2/device2026-04: 2 reports for this device; peer average 2/device2026-05: 0 reports for this device; peer average 1/device0203040708101205071112070905060809101101020406070809100103050810110102030405
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0201
2019-0302
2019-0402
2019-0701
2019-0801
2019-1003
2019-1202
2021-0503
2021-0703
2021-1101
2021-1201
2022-0733
2022-0902
2023-0503
2023-0601
2023-0801
2023-0901
2023-1002
2023-1102
2024-0101
2024-0202
2024-0402
2024-0601
2024-0701
2024-0801
2024-0902
2024-1001
2025-0101
2025-0302
2025-0501
2025-0802
2025-1001
2025-1101.5
2026-0101
2026-0211.5
2026-0302
2026-0422
2026-0501
This device (reports/month)Average device in LZN (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-04-021020279-2026-00463InjuryAvailablecatalog number
2026-02-23MW5184159InjuryAvailablemodel number
2022-07-271020279-2022-03505InjuryAvailablecatalog number

Showing the most recent 3 of 6 linked reports.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2025-01-27NAINo action indicatedIntegrity Orthopaedics Inc0
2023-05-03NAINo action indicatedCARTIHEAL, LTD0
2021-12-09VAIVoluntary action indicatedSmith & Nephew, Inc.1
2021-12-09VAIVoluntary action indicatedSmith & Nephew, Inc.1
2021-10-26NAINo action indicatedSmith & Nephew Inc.0
2021-10-26NAINo action indicatedSmith & Nephew Inc.0
2020-02-06VAIVoluntary action indicatedBlue Belt Technologies, Inc6
2019-10-25NAINo action indicatedTusker Medical, Inc.0
2019-10-08VAIVoluntary action indicatedTusker Medical, Inc.3
2018-03-30NAINo action indicatedAscension Orthopedics, Inc0
2018-02-02NAINo action indicatedSmith & Nephew, Inc.0
2018-02-02NAINo action indicatedSmith & Nephew, Inc.0
2018-01-30NAINo action indicatedSmith & Nephew0
2017-08-21NAINo action indicatedSmith & Nephew, Inc. Advanced Surgical Devices Division0
2017-08-02VAIVoluntary action indicatedSmith & Nephew, Inc.3
2017-08-02VAIVoluntary action indicatedSmith & Nephew, Inc.3
2017-07-24NAINo action indicatedSmith & Nephew, Inc.0
2017-07-24NAINo action indicatedSmith & Nephew, Inc.0
2017-05-25NAINo action indicatedSmith & Nephew, Inc.0
2017-05-25NAINo action indicatedSmith & Nephew, Inc.0
2015-04-30WLWarning LetterSmith & Nephew Inc.
2015-04-30WLWarning LetterSmith & Nephew Inc.
2014-06-11WLWarning LetterSmith & Nephew, Inc.
2010-09-16WLWarning LetterAscension Orthopedics, Inc
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