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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
12232021-09: 0 reports for this device; peer average 3/device2024-09: 1 reports for this device; peer average 1/device2024-10: 1 reports for this device; peer average 1/device090910
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2021-0903
2024-0911
2024-1011
This device (reports/month)Average device in LHC (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
2024-10-223013401749-2024-00001MalfunctionAvailableexact di
2024-09-2520300464MalfunctionAvailablemodel number
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2025-04-22NAINo action indicatedMICROTEK MEDICAL LLC0
2018-06-15NAINo action indicatedMICROTEK MEDICAL LLC0
2016-08-03VAIVoluntary action indicatedMicrotek Medical Inc4
2011-06-22NAINo action indicatedMicrotek Medical Inc0