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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.

25 linked reportsMalfunction 19Injury 6
23562019-01: 0 reports for this device; peer average 1/device2019-06: 0 reports for this device; peer average 1/device2020-04: 0 reports for this device; peer average 1/device2020-07: 0 reports for this device; peer average 1/device2020-10: 0 reports for this device; peer average 1/device2021-01: 0 reports for this device; peer average 3/device2021-02: 0 reports for this device; peer average 1/device2021-03: 0 reports for this device; peer average 1/device2021-10: 1 reports for this device; peer average 1/device2022-01: 1 reports for this device; peer average 1/device2022-04: 1 reports for this device; peer average 1/device2023-02: 5 reports for this device; peer average 5/device2023-03: 2 reports for this device; peer average 1.5/device2023-04: 1 reports for this device; peer average 1/device2023-06: 2 reports for this device; peer average 2/device2023-10: 1 reports for this device; peer average 1/device2024-01: 0 reports for this device; peer average 1/device2024-02: 2 reports for this device; peer average 2/device2024-04: 0 reports for this device; peer average 1/device2024-06: 1 reports for this device; peer average 1/device2024-10: 0 reports for this device; peer average 1/device2025-01: 0 reports for this device; peer average 1/device2025-04: 0 reports for this device; peer average 1/device2025-06: 1 reports for this device; peer average 1/device2025-07: 1 reports for this device; peer average 1/device2025-11: 6 reports for this device; peer average 6/device2025-12: 0 reports for this device; peer average 3/device2026-01: 0 reports for this device; peer average 1/device2026-02: 0 reports for this device; peer average 2/device2026-04: 0 reports for this device; peer average 1/device2026-06: 0 reports for this device; peer average 2/device01060407100102031001040203040610010204061001040607111201020406
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0101
2019-0601
2020-0401
2020-0701
2020-1001
2021-0103
2021-0201
2021-0301
2021-1011
2022-0111
2022-0411
2023-0255
2023-0321.5
2023-0411
2023-0622
2023-1011
2024-0101
2024-0222
2024-0401
2024-0611
2024-1001
2025-0101
2025-0401
2025-0611
2025-0711
2025-1166
2025-1203
2026-0101
2026-0202
2026-0401
2026-0602
This device (reports/month)Average device in IKZ (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2025-11-210001831750-2025-00743MalfunctionAvailableexact di
2025-11-210001831750-2025-00746MalfunctionAvailableexact di
2025-11-210001831750-2025-00745MalfunctionAvailableexact di
2025-11-210001831750-2025-00744MalfunctionAvailableexact di
2025-11-210001831750-2025-00748MalfunctionAvailableexact di
2025-11-210001831750-2025-00747MalfunctionAvailableexact di
2025-07-280001831750-2025-00717MalfunctionAvailableexact di
2025-06-250001831750-2025-00711MalfunctionAvailableexact di
2024-06-280001831750-2024-00727MalfunctionAvailableexact di
2024-02-210001831750-2024-00315MalfunctionAvailableexact di
2024-02-090001831750-2024-00306MalfunctionAvailableexact di
2023-10-240001831750-2023-01248MalfunctionAvailableexact di
2023-06-280001831750-2023-00676MalfunctionAvailableexact di
2023-06-280001831750-2023-00675MalfunctionAvailableexact di
2023-04-170001831750-2023-00340InjuryAvailableexact di
Showing 115 of 25
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2026-06-18NAINo action indicatedInternational Life Sciences0
2026-02-20VAIVoluntary action indicatedStryker Puerto Rico, LLC2
2025-12-11NAINo action indicatedStryker Manufacturing Kalamazoo0
2025-05-22NAINo action indicatedStryker Macroom0
2025-03-27VAIVoluntary action indicatedStryker GmbH1
2025-03-27VAIVoluntary action indicatedStryker GmbH1
2025-02-27NAINo action indicatedStryker Leibinger GmbH & Co. KG0
2025-01-30NAINo action indicatedSerf0
2024-12-18VAIVoluntary action indicatedStryker Neurovascular1
2024-11-15VAIVoluntary action indicatedStryker Medical Division of Stryker Corporation2
2024-11-13NAINo action indicatedPOM Medical LLC0
2024-07-25VAIVoluntary action indicatedStryker Ireland, Ltd., Instruments Division1
2024-05-03NAINo action indicatedStryker Neurovascular, Inc.0
2024-04-18NAINo action indicatedPhysio-Control, Inc.0
2023-12-01VAIVoluntary action indicatedHowmedica Osteonics Corp.1
2023-05-15VAIVoluntary action indicatedLimFlow, Inc.2
2023-04-25NAINo action indicatedStryker Puerto Rico, LLC0
2023-01-24VAIVoluntary action indicatedStryker Corporation2
2023-01-24VAIVoluntary action indicatedStryker Corporation2
2022-03-08VAIVoluntary action indicatedPOM Medical LLC0
2017-04-06WLWarning LetterEntellus Medical Inc.
2015-04-08WLWarning LetterThermedx LLC
2013-11-26INJInjunctionPhysio-Control, Inc.
2013-03-06WLWarning LetterStryker Corporation
2013-03-06WLWarning LetterStryker Corporation
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