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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.

117 linked reportsMalfunction 116Injury 1
24572019-01: 2 reports for this device; peer average 2/device2019-04: 2 reports for this device; peer average 2/device2019-07: 5 reports for this device; peer average 5/device2019-10: 4 reports for this device; peer average 4/device2020-01: 5 reports for this device; peer average 5/device2020-04: 4 reports for this device; peer average 4/device2020-07: 3 reports for this device; peer average 3/device2020-10: 4 reports for this device; peer average 4/device2020-12: 1 reports for this device; peer average 1/device2021-01: 4 reports for this device; peer average 4/device2021-04: 4 reports for this device; peer average 4/device2021-07: 5 reports for this device; peer average 5/device2021-10: 5 reports for this device; peer average 5/device2022-01: 3 reports for this device; peer average 3/device2022-04: 4 reports for this device; peer average 4/device2022-07: 4 reports for this device; peer average 4/device2022-10: 3 reports for this device; peer average 3/device2023-01: 7 reports for this device; peer average 7/device2023-03: 1 reports for this device; peer average 1/device2023-04: 3 reports for this device; peer average 3/device2023-07: 3 reports for this device; peer average 3/device2023-10: 5 reports for this device; peer average 5/device2024-01: 4 reports for this device; peer average 4/device2024-04: 4 reports for this device; peer average 4/device2024-07: 4 reports for this device; peer average 4/device2024-10: 7 reports for this device; peer average 7/device2025-01: 4 reports for this device; peer average 4/device2025-04: 5 reports for this device; peer average 5/device2025-10: 3 reports for this device; peer average 3/device2026-01: 3 reports for this device; peer average 3/device2026-04: 2 reports for this device; peer average 2/device01040710010407101201040710010407100103040710010407100104100104
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0122
2019-0422
2019-0755
2019-1044
2020-0155
2020-0444
2020-0733
2020-1044
2020-1211
2021-0144
2021-0444
2021-0755
2021-1055
2022-0133
2022-0444
2022-0744
2022-1033
2023-0177
2023-0311
2023-0433
2023-0733
2023-1055
2024-0144
2024-0444
2024-0744
2024-1077
2025-0144
2025-0455
2025-1033
2026-0133
2026-0422
This device (reports/month)Average device in HDD (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
2026-04-230001831750-2026-99248MalfunctionAvailableexact di
2026-04-230001831750-2026-99252MalfunctionAvailableexact di
2026-01-270001831750-2026-99131MalfunctionAvailableexact di
2026-01-270001831750-2026-99133MalfunctionAvailableexact di
2026-01-270001831750-2026-99132MalfunctionAvailableexact di
2025-10-270001831750-2025-99344MalfunctionAvailableexact di
2025-10-270001831750-2025-99347MalfunctionAvailableexact di
2025-10-270001831750-2025-99349MalfunctionAvailableexact di
2025-04-280001831750-2025-00600MalfunctionAvailableexact di
2025-04-280001831750-2025-00595MalfunctionAvailableexact di
2025-04-280001831750-2025-00593MalfunctionAvailableexact di
2025-04-280001831750-2025-00631MalfunctionAvailableexact di
2025-04-280001831750-2025-00615MalfunctionAvailableexact di
2025-01-300001831750-2025-00317MalfunctionAvailableexact di
2025-01-280001831750-2025-00164MalfunctionAvailableexact di
Showing 115 of 117
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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