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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.

3 linked reportsMalfunction 2Injury 1
01122021-02: 1 reports for this device; peer average 1/device2026-05: 1 reports for this device; peer average 1.5/device2026-06: 1 reports for this device; peer average 1/device020506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2021-0211
2026-0511.5
2026-0611
This device (reports/month)Average device in LYZ (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
2026-06-301417592-2026-03698Malfunctionexact di
2026-05-011417592-2026-00649MalfunctionAvailableexact di
2021-02-241417592-2021-00025InjuryAvailableexact di
Regulatory clearances

None linked.

Manufacturer compliance record

None in the loaded window.

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