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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
2018-03-01VAIVoluntary action indicatedHighridge Medical LLC2
2018-03-01VAIVoluntary action indicatedHighridge Medical LLC2
2017-09-14NAINo action indicatedHighridge Medical LLC0
2014-12-04NAINo action indicatedLDR Medical0
2014-10-06VAIVoluntary action indicatedHighridge Medical LLC4
2014-10-06VAIVoluntary action indicatedHighridge Medical LLC4
2011-02-24NAINo action indicatedHighridge Medical LLC0
2011-02-24NAINo action indicatedHighridge Medical LLC0
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