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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.

1 linked reportMalfunction 1
142841552019-05: 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 1.5/device2019-09: 0 reports for this device; peer average 1/device2019-11: 0 reports for this device; peer average 1.5/device2019-12: 0 reports for this device; peer average 1/device2020-01: 0 reports for this device; peer average 1/device2020-02: 0 reports for this device; peer average 1.25/device2020-03: 0 reports for this device; peer average 1/device2020-04: 0 reports for this device; peer average 1/device2020-05: 0 reports for this device; peer average 1/device2020-07: 0 reports for this device; peer average 1/device2020-08: 0 reports for this device; peer average 1/device2020-09: 0 reports for this device; peer average 1/device2020-11: 0 reports for this device; peer average 1/device2020-12: 0 reports for this device; peer average 1/device2021-03: 0 reports for this device; peer average 1/device2021-04: 0 reports for this device; peer average 1/device2021-05: 0 reports for this device; peer average 1/device2021-06: 0 reports for this device; peer average 2.67/device2021-07: 0 reports for this device; peer average 1.67/device2021-08: 0 reports for this device; peer average 1/device2021-10: 0 reports for this device; peer average 3.33/device2022-09: 0 reports for this device; peer average 9/device2023-02: 0 reports for this device; peer average 6/device2024-01: 0 reports for this device; peer average 3/device2024-06: 0 reports for this device; peer average 3/device2025-01: 0 reports for this device; peer average 2/device2025-11: 0 reports for this device; peer average 3/device2025-12: 0 reports for this device; peer average 55/device2026-01: 1 reports for this device; peer average 1/device2026-05: 0 reports for this device; peer average 7/device0507080911120102030405070809111203040506070810090201060111120105
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0501
2019-0701
2019-0801.5
2019-0901
2019-1101.5
2019-1201
2020-0101
2020-0201.25
2020-0301
2020-0401
2020-0501
2020-0701
2020-0801
2020-0901
2020-1101
2020-1201
2021-0301
2021-0401
2021-0501
2021-0602.67
2021-0701.67
2021-0801
2021-1003.33
2022-0909
2023-0206
2024-0103
2024-0603
2025-0102
2025-1103
2025-12055
2026-0111
2026-0507
This device (reports/month)Average device in MMK (reports/device/month)
Failure-mode summaryAI-generated

1 linked report narrative available — no AI summary generated yet.

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-01-133003674698-2026-00182MalfunctionAvailableexact di
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2024-01-18NAINo action indicatedMedsource International LLC0
2017-01-06VAIVoluntary action indicatedMedsource International LLC3
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