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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
11222019-01: 0 reports for this device; peer average 1/device2019-04: 0 reports for this device; peer average 1.33/device2019-05: 0 reports for this device; peer average 1.25/device2019-08: 1 reports for this device; peer average 1.5/device2019-09: 0 reports for this device; peer average 1.33/device2019-10: 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 1.5/device2022-01: 0 reports for this device; peer average 1.5/device2022-03: 0 reports for this device; peer average 1.5/device2022-06: 0 reports for this device; peer average 1.5/device2023-04: 0 reports for this device; peer average 1/device2023-08: 0 reports for this device; peer average 1.5/device2024-06: 0 reports for this device; peer average 1.5/device2024-07: 0 reports for this device; peer average 2.25/device2024-09: 0 reports for this device; peer average 1/device2024-10: 0 reports for this device; peer average 2/device2025-06: 0 reports for this device; peer average 1/device2025-08: 0 reports for this device; peer average 1.5/device01040508091012010103060408060709100608
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0101
2019-0401.33
2019-0501.25
2019-0811.5
2019-0901.33
2019-1001.5
2019-1201
2020-0101.5
2022-0101.5
2022-0301.5
2022-0601.5
2023-0401
2023-0801.5
2024-0601.5
2024-0702.25
2024-0901
2024-1002
2025-0601
2025-0801.5
This device (reports/month)Average device in ETA (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
2019-08-141045254-2019-00383MalfunctionAvailablemodel number
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2024-06-17VAIVoluntary action indicatedMedtronic Xomed, Inc.1
2021-10-29VAIVoluntary action indicatedMedtronic Xomed, Inc.5
2015-09-21VAIVoluntary action indicatedMedtronic Xomed, Inc.1
2012-07-03VAIVoluntary action indicatedMedtronic Xomed, Inc.8
2012-06-06NAINo action indicatedMedtronic Xomed, Inc.0
2010-08-05VAIVoluntary action indicatedMedtronic Xomed, Inc.4
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