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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 3
12232021-10: 3 reports for this device; peer average 3/device10
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2021-1033
This device (reports/month)Average device in NDL (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2021-10-222031009-2021-00005MalfunctionAvailablecatalog number

Showing the most recent 1 of 3 linked reports.

Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2024-06-03VAIVoluntary action indicatedTriMed Inc.2
2024-06-03VAIVoluntary action indicatedTriMed Inc.2
2019-08-14NAINo action indicatedTriMed Inc.0
2019-08-14NAINo action indicatedTriMed Inc.0
2017-11-17VAIVoluntary action indicatedTriMed Inc.6
2017-11-17VAIVoluntary action indicatedTriMed Inc.6
2017-01-12VAIVoluntary action indicatedTriMed Inc.11
2017-01-12VAIVoluntary action indicatedTriMed Inc.11
2016-06-30WLWarning LetterTriMed Inc.
2016-06-30WLWarning LetterTriMed Inc.
2016-03-18OAIOfficial action indicatedTriMed Inc.13
2016-03-18OAIOfficial action indicatedTriMed Inc.13
2012-01-25VAIVoluntary action indicatedTriMed Inc.5
2012-01-25VAIVoluntary action indicatedTriMed Inc.5
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