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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
2024-01-12VAIVoluntary action indicatedNational Advanced Endoscopy Devices Inc0
2024-01-12VAIVoluntary action indicatedNational Advanced Endoscopy Devices Inc0
2020-09-03VAIVoluntary action indicatedNational Advanced Endoscopy Devices Inc1
2020-09-03VAIVoluntary action indicatedNational Advanced Endoscopy Devices Inc1
2019-08-30VAIVoluntary action indicatedNational Advanced Endoscopy Devices Inc1
2019-08-30VAIVoluntary action indicatedNational Advanced Endoscopy Devices Inc1
2015-10-26VAIVoluntary action indicatedNational Advanced Endoscopy Devices Inc3
2015-10-26VAIVoluntary action indicatedNational Advanced Endoscopy Devices Inc3
2012-07-17NAINo action indicatedNational Advanced Endoscopy Devices Inc0
2012-07-17NAINo action indicatedNational Advanced Endoscopy Devices Inc0
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