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.

15 linked reportsMalfunction 12Injury 3
12232019-02: 0 reports for this device; peer average 1/device2019-07: 1 reports for this device; peer average 1/device2019-08: 1 reports for this device; peer average 1/device2019-10: 0 reports for this device; peer average 3/device2021-06: 3 reports for this device; peer average 3/device2021-07: 1 reports for this device; peer average 2/device2022-07: 1 reports for this device; peer average 1/device2023-10: 2 reports for this device; peer average 2/device2024-02: 0 reports for this device; peer average 2/device2024-04: 0 reports for this device; peer average 2/device2024-10: 1 reports for this device; peer average 1/device2025-01: 1 reports for this device; peer average 1/device2025-03: 0 reports for this device; peer average 2/device2025-04: 1 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/device2026-05: 1 reports for this device; peer average 1/device0207081006070710020410010304060705
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0201
2019-0711
2019-0811
2019-1003
2021-0633
2021-0712
2022-0711
2023-1022
2024-0202
2024-0402
2024-1011
2025-0111
2025-0302
2025-0411
2025-0611
2025-0711
2026-0511
This device (reports/month)Average device in JDK (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-05-0625093303MalfunctionAvailableprocode brand trgm
2025-07-243015967359-2025-99051MalfunctionAvailableexact di
2025-06-173015967359-2025-01120InjuryAvailableexact di
2025-04-213015967359-2025-00916MalfunctionAvailableexact di
2025-01-213015967359-2025-00141MalfunctionAvailableexact di
2024-10-223015967359-2024-02215MalfunctionAvailableexact di
2023-10-233015967359-2023-02157MalfunctionAvailableexact di
2023-10-233015967359-2023-02185MalfunctionAvailableexact di
2022-07-263015967359-2022-01516MalfunctionAvailableexact di
2021-07-193015967359-2021-01442InjuryAvailableexact di
2021-06-1111982737MalfunctionAvailablecatalog number
2019-08-080001811755-2019-02671MalfunctionAvailableexact di
2019-07-290001811755-2019-02588InjuryAvailableexact di

Showing the most recent 13 of 15 linked reports.

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
Similar devices
Select up to two to place side-by-side with this device.