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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.

2 linked reportsMalfunction 2
11232021-03: 0 reports for this device; peer average 1/device2021-10: 0 reports for this device; peer average 1/device2022-02: 0 reports for this device; peer average 1/device2022-04: 0 reports for this device; peer average 1/device2022-05: 0 reports for this device; peer average 1/device2022-09: 0 reports for this device; peer average 1/device2022-10: 0 reports for this device; peer average 1/device2023-01: 0 reports for this device; peer average 2/device2023-02: 0 reports for this device; peer average 1/device2023-03: 0 reports for this device; peer average 2/device2023-04: 0 reports for this device; peer average 1/device2023-05: 2 reports for this device; peer average 1.33/device2023-06: 0 reports for this device; peer average 1/device2023-10: 0 reports for this device; peer average 1/device2023-11: 0 reports for this device; peer average 1/device2023-12: 0 reports for this device; peer average 1/device2024-02: 0 reports for this device; peer average 1/device2024-03: 0 reports for this device; peer average 1/device2024-05: 0 reports for this device; peer average 1/device2024-08: 0 reports for this device; peer average 2/device2024-09: 0 reports for this device; peer average 1/device2024-12: 0 reports for this device; peer average 2/device2025-04: 0 reports for this device; peer average 2.5/device2025-07: 0 reports for this device; peer average 1/device2025-08: 0 reports for this device; peer average 1.5/device2025-10: 0 reports for this device; peer average 1/device2026-01: 0 reports for this device; peer average 1/device2026-03: 0 reports for this device; peer average 1/device2026-04: 0 reports for this device; peer average 1/device0310020405091001020304050610111202030508091204070810010304
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2021-0301
2021-1001
2022-0201
2022-0401
2022-0501
2022-0901
2022-1001
2023-0102
2023-0201
2023-0302
2023-0401
2023-0521.33
2023-0601
2023-1001
2023-1101
2023-1201
2024-0201
2024-0301
2024-0501
2024-0802
2024-0901
2024-1202
2025-0402.5
2025-0701
2025-0801.5
2025-1001
2026-0101
2026-0301
2026-0401
This device (reports/month)Average device in HNQ (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2023-05-31MW5118027MalfunctionAvailablecatalog number

Showing the most recent 1 of 2 linked reports.

Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2016-08-31NAINo action indicatedKatena Products, Inc.0
2014-04-21NAINo action indicatedKatena Products Inc.0
2012-02-22NAINo action indicatedKatena Products, Inc.0
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