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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.

No adverse-event reports are linked to this device.

Recall history

No recalls linked.

Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2025-05-22VAIVoluntary action indicatedClarus Medical, Llc3
2025-05-22VAIVoluntary action indicatedClarus Medical, Llc3
2021-03-10NAINo action indicatedClarus Medical, Llc1
2021-03-10NAINo action indicatedClarus Medical, Llc1
2018-08-23VAIVoluntary action indicatedClarus Medical, Llc1
2018-08-23VAIVoluntary action indicatedClarus Medical, Llc1
2015-04-13NAINo action indicatedClarus Medical, Llc0
2015-04-13NAINo action indicatedClarus Medical, Llc0
2011-07-25NAINo action indicatedClarus Medical, Llc2
2011-07-25NAINo action indicatedClarus Medical, Llc2
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